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Translation Factor: EEF2 (NCBI Gene ID:1938) |
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Gene Information | Gene Name: EEF2 | Gene ID: 1938 | Gene Symbol | EEF2 | Gene ID | 1938 |
Gene Name | eukaryotic translation elongation factor 2 | |
Synonyms | EEF-2|EF-2|EF2|SCA26 | |
Cytomap | 19p13.3 | |
Type of Gene | protein-coding | |
Description | elongation factor 2epididymis secretory sperm binding proteinpolypeptidyl-tRNA translocase | |
Modification date | 20200313 | |
UniProtAcc | P13639 |
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GO ID | GO term |
GO:0006417 | Regulation of translation |
GO:0008135 | Translation factor activity, RNA binding |
GO:0045727 | Positive regulation of translation |
GO:0006414 | Translational elongation |
GO:0006412 | Translation |
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Partner | Gene | GO ID | GO term | PubMed ID |
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Gene | Inferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25 |
EEF2 | >1119.25 |
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Gene | Title | PMID |
EEF2 | dentification and characterization of a novel evolutionarily conserved lysine-specific methyltransferase targeting eukaryotic translation elongation factor 2 (eEF2) | 25231979 |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. For more annotations, please visit our ExonSkipDB. |
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![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ENST | Exon skip start (DNA) | Exon Skip end (DNA) | ORF |
ENST00000309311 | 3977212 | 3977345 | Frame-shift |
ENST00000309311 | 3977425 | 3977608 | In-frame |
ENST00000309311 | 3977816 | 3978170 | In-frame |
ENST00000309311 | 3979805 | 3980064 | Frame-shift |
ENST00000309311 | 3981336 | 3981450 | In-frame |
ENST00000309311 | 3984133 | 3984348 | Frame-shift |
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ENST | Exon skip start (DNA) | Exon Skip end (DNA) | Len(transcript seq) | Exon skip start (mRNA) | Exon Skip end (mRNA) | Len(amino acid seq) | Exon skip start (AA) | Exon Skip end (AA) |
ENST00000309311 | 3977425 | 3977608 | 3181 | 2157 | 2339 | 858 | 689 | 750 |
ENST00000309311 | 3977816 | 3978170 | 3181 | 1803 | 2156 | 858 | 571 | 689 |
ENST00000309311 | 3981336 | 3981450 | 3181 | 987 | 1100 | 858 | 299 | 337 |
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UniProtAcc | Exon skip start (AA) | Exon Skip end (AA) | Function feature start (AA) | Function feature end (AA) | Functional feature type | Functional feature desc. |
P13639 | 689 | 750 | 2 | 858 | Chain | ID=PRO_0000091000;Note=Elongation factor 2 |
P13639 | 571 | 689 | 2 | 858 | Chain | ID=PRO_0000091000;Note=Elongation factor 2 |
P13639 | 299 | 337 | 2 | 858 | Chain | ID=PRO_0000091000;Note=Elongation factor 2 |
P13639 | 299 | 337 | 17 | 362 | Domain | Note=tr-type G;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU01059 |
P13639 | 571 | 689 | 586 | 587 | Site | Note=Cleavage;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518 |
P13639 | 571 | 689 | 605 | 606 | Site | Note=Cleavage;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518 |
P13639 | 299 | 337 | 325 | 325 | Modified residue | Note=Phosphoserine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P05197 |
P13639 | 571 | 689 | 572 | 572 | Modified residue | Note=N6-succinyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P58252 |
P13639 | 571 | 689 | 595 | 595 | Modified residue | Note=Phosphoserine%3B by CDK2;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:23184662;Dbxref=PMID:23186163,PMID:23184662 |
P13639 | 571 | 689 | 619 | 619 | Modified residue | Note=N6-acetyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P58252 |
P13639 | 689 | 750 | 715 | 715 | Modified residue | Note=Diphthamide;Ontology_term=ECO:0000250;evidence=ECO:0000250 |
P13639 | 299 | 337 | 322 | 322 | Cross-link | Note=Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO);Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24648518;Dbxref=PMID:24648518 |
P13639 | 571 | 689 | 596 | 596 | Natural variant | ID=VAR_070792;Note=In SCA26%3B compromises the mechanics of translocation. P->H;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23001565;Dbxref=dbSNP:rs587777052,PMID:23001565 |
P13639 | 571 | 689 | 595 | 595 | Mutagenesis | Note=Strongly reduced phosphorylation at Thr-57. S->A;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23184662;Dbxref=PMID:23184662 |
P13639 | 571 | 689 | 599 | 599 | Mutagenesis | Note=Strongly reduced phosphorylation at Thr-57. H->P;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23184662;Dbxref=PMID:23184662 |
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Cancer type | Translation factor | FC | adj.pval |
HNSC | EEF2 | -1.90805330069302 | 0.000299885096865183 |
THCA | EEF2 | 1.35574858496176 | 0.000711089919756285 |
COAD | EEF2 | 1.67025113686866 | 0.00197160243988037 |
STAD | EEF2 | -1.87846190344448 | 0.00733334058895707 |
ESCA | EEF2 | -3.4598326417414 | 0.0185546875 |
PRAD | EEF2 | 1.63926479894191 | 2.70126293247147e-08 |
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Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
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Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
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Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
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Cancer type | Gene | Coefficient | Pvalue |
OV | EEF2 | -0.071438621 | 0.045524397 |
KIRC | EEF2 | -0.05048307 | 0.045613842 |
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Cancer type | Gene group | Translation factor | Correlated gene | Coefficient | Pvalue |
LAML | TSG | EEF2 | GNB2L1 | 0.811723162 | 8.63E-42 |
LAML | TSG | EEF2 | GLTSCR2 | 0.841836515 | 1.15E-47 |
TGCT | TF | EEF2 | ZNF490 | 0.807226242 | 4.34E-37 |
UVM | Cell metabolism gene | EEF2 | IMPDH2 | 0.830609759 | 1.59E-21 |
UVM | Epifactor | EEF2 | TRIM28 | 0.801421521 | 4.33E-19 |
UVM | Epifactor | EEF2 | FBL | 0.807414939 | 1.48E-19 |
UVM | IUPHAR | EEF2 | TRIM28 | 0.801421521 | 4.33E-19 |
UVM | IUPHAR | EEF2 | IMPDH2 | 0.830609759 | 1.59E-21 |
UVM | Kinase | EEF2 | TRIM28 | 0.801421521 | 4.33E-19 |
UVM | TF | EEF2 | ZNF581 | 0.804324401 | 2.58E-19 |
UVM | TSG | EEF2 | GLTSCR2 | 0.824947293 | 5.10E-21 |
UVM | TSG | EEF2 | GNB2L1 | 0.857051557 | 3.59E-24 |
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![]() Visit iCn3D. |
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![]() * Overlap between up-regulated DEGs (log2FC<-1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P)) |
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![]() * Edge colors based on TCGA cancer types. |
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Cancer type | Translation factor | Interacting protein coding gene | FC | adj.pval |
KIRP | EEF2 | RPL18A | -1.51651392808885 | 0.00016188295558095 |
KIRP | EEF2 | RPS16 | -1.35957043617517 | 0.00019507110118866 |
COAD | EEF2 | RPS3 | 1.48730375143014 | 0.000411599874496461 |
COAD | EEF2 | RPL13 | 2.11745314482912 | 0.000465095043182374 |
LIHC | EEF2 | RPL8 | -4.84588284974558 | 0.00110314154326131 |
THCA | EEF2 | RPL4 | 1.38794063541307 | 0.00128543522995411 |
PRAD | EEF2 | RPL4 | 1.2589775892273 | 0.00136912931788367 |
PRAD | EEF2 | RPL18A | 1.40600175748499 | 0.00205137828390396 |
KICH | EEF2 | RPL19 | 1.36901182894089 | 0.00250792503356934 |
KICH | EEF2 | RPLP2 | -2.79941030721041 | 0.00250792503356934 |
ESCA | EEF2 | RPL15 | 1.76629417535644 | 0.0048828125 |
STAD | EEF2 | RPL4 | 1.50541710129002 | 0.00647870777174831 |
LUAD | EEF2 | RPL19 | -1.31398026615725 | 0.00993159558412698 |
THCA | EEF2 | RPS16 | -6.16322798156577 | 0.0115764821363307 |
BLCA | EEF2 | RPL4 | -1.27208291287992 | 0.0180816650390625 |
HNSC | EEF2 | RPS3 | -4.73505819095135 | 0.0273726439852453 |
STAD | EEF2 | RPL13 | -1.17078722854876 | 0.0294188209809363 |
COAD | EEF2 | RPLP2 | 1.74101665732582 | 0.0334101617336274 |
KICH | EEF2 | RPL13 | -5.95618047175394 | 0.0366820693016052 |
COAD | EEF2 | RPS9 | 1.18612014402235 | 0.0381683111190796 |
LUSC | EEF2 | RPL19 | -2.14669889516666 | 0.044366810398747 |
KIRC | EEF2 | RPL19 | -2.73485271276676 | 1.33980982873695e-10 |
BRCA | EEF2 | RPS9 | 1.9331477546349 | 2.31299392089389e-07 |
KIRC | EEF2 | RPL13 | -3.44015571111292 | 2.58914497097505e-10 |
KIRC | EEF2 | RPL4 | -2.62009040507781 | 3.30026076039221e-08 |
KIRC | EEF2 | RPLP2 | -1.31294149421946 | 3.74941832864519e-08 |
KIRC | EEF2 | RPL8 | -1.18252459971773 | 5.64962994208288e-07 |
KIRP | EEF2 | RPL8 | -1.53003692350119 | 6.0301274061203e-05 |
KIRP | EEF2 | RPLP2 | -1.33740048133375 | 6.0301274061203e-05 |
KIRC | EEF2 | RPS9 | -1.32680816440987 | 6.53264115309597e-07 |
KIRC | EEF2 | RPS16 | -1.66149869889384 | 7.8509870430991e-09 |
KIRC | EEF2 | RPS3 | -1.29560847926387 | 9.05905681935088e-10 |
KIRC | EEF2 | RPL18A | -4.43079304960843 | 9.2516163152192e-11 |
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PPI interactors with EEF2 |
TP53, MLLT3, POU5F1, UCHL5, Mapk13, PPP2R1A, PPP2R1B, NOP56, DISC1, PSMA3, NDRG1, HDGF, ARRB2, ISG15, FBXO25, EEF2K, CUL3, CUL4B, CUL5, CDK2, CUL1, COPS5, COPS6, CAND1, GRK5, RAD23A, RPL5, RPS6, RPS3A, RPL7, RPS4X, RPL7A, EEF1A1, RPS16, RPS23, RPL31, RPS24, RPL12, RPL4, RPS15A, RPL10A, RPL14, RPL6, RPL18, RPS7, RPL21, RPL11, RPL23, RPS2, RPS5, RPS19, TARS, MRPS5, HSPD1, HSPA8, EIF4A1, PABPC1, FARSA, RPLP0P6, XRCC6, RPL10L, FLOT2, RRM1, HNRNPA0, EPHA2, ERLIN2, RBM4, HNRNPH1, RHOT2, HNRNPDL, HNRNPL, DDX5, ATP6V1H, NUP62, HNRNPA3, UPF1, SMURF1, CCT2, HSP90AA1, HSP90AB1, FN1, VCAM1, ATF2, MLH1, EEF2KMT, UBL4A, ITGA4, NPM1, SMG1, ADRB2, HNRNPD, MAPK14, HIPK4, CDK18, CDK20, TARDBP, CDKN2A, BZW1, CASP7, CKB, CAPN1, FTO, GSR, PGD, TYMP, EIF4H, GINS2, MAT2A, PAK2, PFAS, RPS6KA1, XPO1, YWHAQ, SHFM1, LGR4, EFM3, HUWE1, FUS, MDM2, RNF2, SIRT6, ARAF, BLK, BUB1B, CASK, CDK13, DAPK1, IRAK1, LIMK2, WEE1, ESR1, HNRNPA1, UNK, EP300, CALR, ABCC3, ABCD3, AHNAK, ARPC2, ATIC, ATP1B3, AURKA, CASP3, CSE1L, DPH1, DPH2, EEF1A2, ENO1, GSPT1, HSD17B10, NDUFV1, NOTCH2, PGK1, TAGLN, TAGLN2, TOMM40, TXN, HCFC1, HSD17B4, IPO4, ISYNA1, OPA1, RDX, TUBB, NTRK1, PTEN, PPME1, Cct3, GAN, CRY1, CRY2, MCM2, SENP3, U2AF2, NFATC2, CDC73, WWP2, ZNF746, CDH1, FBXO9, DEFA1, SLC25A48, CYLD, DLD, DLST, DNM1L, PARK7, SDHA, SOAT1, SOD1, VDAC1, TRIM25, BRCA1, HDAC6, CFTR, CPEB2, ZNF598, KEAP1, EGLN3, ADSS, JUP, PCBP1, PPP6C, COPE, CTNNB1, GALE, IGF1R, KRAS, TGFB1, YAF2, YAP1, UBE2M, PRPF8, EFTUD2, AAR2, PIH1D1, AKTIP, RNF4, TNF, CDC34, HEXIM1, MEPCE, LARP7, PPT1, NBN, SNAI1, AGR2, RECQL4, DCPS, RNF144A, ZFP36L2, MYC, CDC37, NEK2, GRWD1, KRT17, METTL3, METTL14, KIAA1429, USP18, RC3H2, ATG16L1, ACTC1, PHB, FAF1, RBX1, NR2C2, UBQLN2, UBE3C, HDAC2, AGRN, BMH2, BMH1, ATXN3, VRK3, HMOX2, ATP6V1B2, UQCRC2, LRRC59, PDHA1, PHB2, APOE, UQCRC1, NDUFS7, POR, AGPS, PDHB, NDUFS8, BCKDHA, ATP5B, NNT, NDUFS3, P4HA1, EMC8, HADHA, CYC1, CANX, EMC2, ASPH, NDUFA8, ATP6V1A, LONP1, NIPSNAP1, UQCRH, RCN2, TUFM, MGST1, EMC4, PRDX3, OGDH, NCF1, ITFG1, GSK3B, BIRC3, NFX1, BRD7, UBC, SOX2, PARK2, PPIA, ARIH2, PLEKHA4, PINK1, TFCP2, FANCD2, LINC01554, ZC3H18, FYN, GRB2, LCK, RAC1, SH3GL3, SHC1, NME1, ANKRD55, NEK4, DUX4, CIT, ANLN, CHMP4C, KIF14, KIF20A, KIF23, PRC1, PRNP, SUMO2, NDN, BIN1, BRD4, RBM45, CIC, Apc2, RBM39, FBP1, LGALS9, CSPG4, IFI16, CREBBP, INSIG1, USP15, RIN3, DDX58, BAG5, AR, UFL1, DDRGK1, LINC00152, TRIM37, FZR1, WDR5, PAGE4, BGLT3, HSPA1A, DTX3, SPRTN, USP11, BTF3, FBXW7, NLRP7, LHPP, E, nsp1, nsp12, nsp14, nsp15, nsp8, ORF3a, ORF7b, KDM4C, HECTD1, MAP1LC3B, CALCOCO2, SQSTM1, ANTXR1, PER2, MAGEL2, |
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Gene | Chr | Position | RefSeq | VarSeq | RefSeeq | VarType | Pathogenic | Disease | VarInfo |
EEF2 | chr19 | 3976253 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001624|3_prime_UTR_variant | SO:0001624|3_prime_UTR_variant |
EEF2 | chr19 | 3976321 | T | G | single_nucleotide_variant | Benign | not_provided | SO:0001624|3_prime_UTR_variant | SO:0001624|3_prime_UTR_variant |
EEF2 | chr19 | 3976441 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001624|3_prime_UTR_variant | SO:0001624|3_prime_UTR_variant |
EEF2 | chr19 | 3976549 | C | T | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001624|3_prime_UTR_variant | SO:0001624|3_prime_UTR_variant |
EEF2 | chr19 | 3976599 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976633 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976666 | G | A | single_nucleotide_variant | Likely_benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976669 | C | A | single_nucleotide_variant | Likely_benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976669 | C | G | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976680 | A | C | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3976699 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976705 | C | T | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976714 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3976863 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3977205 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3977217 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977265 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977289 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977416 | T | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3977435 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977471 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977471 | G | C | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977486 | A | G | single_nucleotide_variant | Benign | Spinocerebellar_ataxia_type_26|not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977501 | T | C | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977528 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977540 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977543 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977546 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977561 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977567 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977586 | A | G | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3977762 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3977807 | C | T | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3977895 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977905 | T | C | single_nucleotide_variant | not_provided | Spinocerebellar_ataxia_type_26 | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3977953 | G | A | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3977976 | G | C | single_nucleotide_variant | Benign/Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3977988 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978015 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978097 | G | T | single_nucleotide_variant | Pathogenic | Spinocerebellar_ataxia_type_26|not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3978100 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3978114 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978138 | C | G | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978138 | C | T | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978159 | C | T | single_nucleotide_variant | Likely_benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3978176 | A | G | single_nucleotide_variant | Likely_benign | not_specified | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3979156 | G | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3979312 | T | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3979319 | C | A | single_nucleotide_variant | Benign | not_specified | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3979338 | T | C | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3979363 | C | T | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979372 | G | T | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979402 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979408 | A | G | single_nucleotide_variant | Benign | Spinocerebellar_ataxia_type_26|not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979690 | C | CT | Duplication | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3979820 | C | T | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3979842 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979862 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979869 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979932 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979941 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3979965 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980061 | T | C | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980072 | A | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3980367 | G | T | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3980535 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980565 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980607 | G | T | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3980625 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980643 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980682 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980689 | G | A | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3980690 | G | C | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3980714 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_specified|not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3980824 | A | G | single_nucleotide_variant | Benign | Spinocerebellar_ataxia_type_26|not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3980835 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3980839 | C | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3980852 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3980901 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3981320 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3981439 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3981442 | A | G | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3981443 | T | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3981460 | C | T | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3981526 | A | G | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3982005 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982031 | C | T | single_nucleotide_variant | Likely_benign | not_specified | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982041 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982054 | G | C | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3982235 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3982248 | C | G | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982289 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982294 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982323 | C | T | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982324 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982368 | A | G | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982377 | C | T | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982398 | C | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3982402 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982408 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982785 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3982826 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982832 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982847 | G | A | single_nucleotide_variant | Uncertain_significance | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982850 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982874 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982895 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982931 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982967 | G | A | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982973 | G | A | single_nucleotide_variant | Benign/Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3982984 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001587|nonsense | SO:0001587|nonsense |
EEF2 | chr19 | 3983015 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983082 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3983142 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983169 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983184 | A | G | single_nucleotide_variant | Benign | not_specified|not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983190 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983220 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983225 | C | T | single_nucleotide_variant | Likely_benign | not_specified | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3983226 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983229 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983232 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3983302 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3983562 | T | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3983930 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984134 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3984142 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3984199 | G | A | single_nucleotide_variant | Benign | not_specified | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3984209 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3984224 | G | A | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3984238 | G | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3984266 | T | G | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001583|missense_variant | SO:0001583|missense_variant |
EEF2 | chr19 | 3984292 | G | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3984337 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001819|synonymous_variant | SO:0001819|synonymous_variant |
EEF2 | chr19 | 3984351 | G | C | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984356 | A | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984412 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984453 | G | A | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984489 | C | T | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3984540 | T | C | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3985148 | A | G | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3985242 | C | A | single_nucleotide_variant | Likely_benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3985250 | C | G | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
EEF2 | chr19 | 3985385 | G | C | single_nucleotide_variant | Uncertain_significance | not_provided | SO:0001623|5_prime_UTR_variant | SO:0001623|5_prime_UTR_variant |
EEF2 | chr19 | 3985576 | C | T | single_nucleotide_variant | Benign | not_provided |
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Gene | Cancer type | Chromosome | Start | End | RefSeeq | MutSeq | Mutation type | AAchange | # samples |
EEF2 | KIRP | chr19 | 3979985 | 3979985 | C | T | Missense_Mutation | p.D476N | 10 |
EEF2 | BRCA | chr19 | 3982347 | 3982347 | C | T | Missense_Mutation | p.E230K | 5 |
EEF2 | ESCA | chr19 | 3980633 | 3980633 | G | A | Missense_Mutation | p.R409W | 5 |
EEF2 | STAD | chr19 | 3976713 | 3976713 | C | T | Missense_Mutation | p.G806S | 5 |
EEF2 | KIRP | chr19 | 3979985 | 3979985 | C | T | Missense_Mutation | 4 | |
EEF2 | PAAD | chr19 | 3980040 | 3980040 | G | C | Nonsense_Mutation | p.Y457* | 4 |
EEF2 | SKCM | chr19 | 3982420 | 3982420 | G | A | Silent | p.I205I | 4 |
EEF2 | ESCA | chr19 | 3982015 | 3982015 | G | A | Missense_Mutation | p.S276L | 4 |
EEF2 | UCEC | chr19 | 3979938 | 3979938 | C | T | Silent | p.A491 | 4 |
EEF2 | COAD | chr19 | 3981982 | 3981982 | C | T | Missense_Mutation | p.R287H | 3 |
EEF2 | UCEC | chr19 | 3981983 | 3981983 | G | A | Missense_Mutation | p.R287C | 3 |
EEF2 | UCEC | chr19 | 3982933 | 3982933 | G | A | Missense_Mutation | p.R162C | 3 |
EEF2 | PAAD | chr19 | 3981965 | 3981965 | T | C | Missense_Mutation | p.I293V | 3 |
EEF2 | PAAD | chr19 | 3977529 | 3977529 | C | T | Missense_Mutation | p.R716H | 3 |
EEF2 | BRCA | chr19 | 3982420 | 3982420 | G | C | Missense_Mutation | p.I205M | 3 |
EEF2 | PAAD | chr19 | 3976682 | 3976682 | T | A | Missense_Mutation | p.H816L | 3 |
EEF2 | ESCA | chr19 | 3982015 | 3982015 | G | A | Missense_Mutation | 3 | |
EEF2 | UCEC | chr19 | 3984224 | 3984225 | - | CCTT | Frame_Shift_Ins | p.A43fs | 3 |
EEF2 | ESCA | chr19 | 3980008 | 3980008 | T | C | Missense_Mutation | p.N468S | 3 |
EEF2 | LUAD | chr19 | 3982008 | 3982008 | G | T | Silent | p.T278T | 3 |
EEF2 | THYM | chr19 | 3977539 | 3977539 | C | T | Missense_Mutation | p.A713T | 3 |
EEF2 | ACC | chr19 | 3979353 | 3979353 | C | T | Missense_Mutation | p.E563K | 3 |
EEF2 | COAD | chr19 | 3977486 | 3977486 | A | G | Silent | p.Y730Y | 3 |
EEF2 | ACC | chr19 | 3976662 | 3976662 | C | G | Missense_Mutation | p.D823H | 3 |
EEF2 | ESCA | chr19 | 3982335 | 3982335 | C | A | Missense_Mutation | p.A234S | 3 |
EEF2 | ESCA | chr19 | 3984216 | 3984216 | T | C | Missense_Mutation | p.I46V | 3 |
EEF2 | PRAD | chr19 | 3984203 | 3984203 | C | G | Missense_Mutation | p.R50P | 3 |
EEF2 | PAAD | chr19 | 3981965 | 3981965 | T | C | Missense_Mutation | 2 | |
EEF2 | BLCA | chr19 | 3977234 | 3977234 | G | A | Silent | p.L788L | 2 |
EEF2 | BRCA | chr19 | 3980544 | 3980544 | C | T | Silent | p.K438 | 2 |
EEF2 | ESCA | chr19 | 3982032 | 3982032 | G | A | Silent | p.N270N | 2 |
EEF2 | STAD | chr19 | 3977228 | 3977228 | C | T | Missense_Mutation | p.V790I | 2 |
EEF2 | UCEC | chr19 | 3979994 | 3979994 | C | T | Missense_Mutation | p.V473M | 2 |
EEF2 | PAAD | chr19 | 3980040 | 3980040 | G | C | Nonsense_Mutation | p.Y457X | 2 |
EEF2 | BLCA | chr19 | 3979971 | 3979971 | C | A | Silent | p.V480V | 2 |
EEF2 | COAD | chr19 | 3982314 | 3982314 | C | - | Frame_Shift_Del | p.E241fs | 2 |
EEF2 | BRCA | chr19 | 3983150 | 3983150 | G | C | Missense_Mutation | p.R120G | 2 |
EEF2 | ESCA | chr19 | 3984216 | 3984216 | T | C | Missense_Mutation | 2 | |
EEF2 | SARC | chr19 | 3980914 | 3980914 | G | A | Missense_Mutation | 2 | |
EEF2 | STAD | chr19 | 3982369 | 3982369 | G | T | Silent | p.A222A | 2 |
EEF2 | UCEC | chr19 | 3981438 | 3981438 | T | C | Missense_Mutation | p.I304V | 2 |
EEF2 | STAD | chr19 | 3977945 | 3977945 | G | A | Missense_Mutation | 2 | |
EEF2 | ESCA | chr19 | 3980633 | 3980633 | G | A | Missense_Mutation | 2 | |
EEF2 | UCEC | chr19 | 3982293 | 3982293 | C | T | Missense_Mutation | p.E248K | 2 |
EEF2 | LUAD | chr19 | 3979429 | 3979429 | G | A | Silent | p.I537I | 2 |
EEF2 | STAD | chr19 | 3980044 | 3980044 | C | T | Missense_Mutation | 2 | |
EEF2 | UCEC | chr19 | 3982300 | 3982300 | C | T | Silent | p.G245 | 2 |
EEF2 | HNSC | chr19 | 3977901 | 3977901 | G | A | Silent | p.I661I | 2 |
EEF2 | STAD | chr19 | 3980044 | 3980044 | C | T | Missense_Mutation | p.R456H | 2 |
EEF2 | BLCA | chr19 | 3982047 | 3982047 | G | A | Silent | p.Y265Y | 2 |
EEF2 | UCEC | chr19 | 3982839 | 3982839 | C | T | Missense_Mutation | p.G193D | 2 |
EEF2 | LUAD | chr19 | 3979399 | 3979399 | C | A | Silent | p.A547A | 2 |
EEF2 | STAD | chr19 | 3977945 | 3977945 | G | A | Missense_Mutation | p.R647C | 2 |
EEF2 | CESC | chr19 | 3979965 | 3979965 | C | T | Silent | 2 | |
EEF2 | UCEC | chr19 | 3976618 | 3976618 | C | T | Silent | p.E837 | 2 |
EEF2 | SKCM | chr19 | 3980032 | 3980032 | G | A | Missense_Mutation | p.P460L | 2 |
EEF2 | ESCA | chr19 | 3982335 | 3982335 | C | A | Missense_Mutation | 2 | |
EEF2 | UCEC | chr19 | 3976737 | 3976737 | C | T | Missense_Mutation | p.A798T | 2 |
EEF2 | ESCA | chr19 | 3982032 | 3982032 | G | A | Silent | 2 | |
EEF2 | PAAD | chr19 | 3980040 | 3980040 | G | C | Nonsense_Mutation | 2 | |
EEF2 | STAD | chr19 | 3982022 | 3982022 | T | C | Missense_Mutation | p.S274G | 2 |
EEF2 | SKCM | chr19 | 3977900 | 3977900 | G | A | Missense_Mutation | p.L662F | 2 |
EEF2 | UCEC | chr19 | 3977878 | 3977878 | A | G | Missense_Mutation | p.V669A | 2 |
EEF2 | KIRP | chr19 | 3983291 | 3983293 | TGA | - | Splice_Site | . | 2 |
EEF2 | STAD | chr19 | 3977944 | 3977944 | C | T | Missense_Mutation | p.R647H | 2 |
EEF2 | SKCM | chr19 | 3979426 | 3979426 | G | A | Silent | p.I538I | 2 |
EEF2 | CESC | chr19 | 3978083 | 3978083 | G | A | Missense_Mutation | 2 | |
EEF2 | UCEC | chr19 | 3977918 | 3977918 | C | T | Missense_Mutation | p.G656S | 2 |
EEF2 | PAAD | chr19 | 3977529 | 3977529 | C | T | Missense_Mutation | 2 | |
EEF2 | BRCA | chr19 | 3978146 | 3978146 | G | A | Missense_Mutation | p.R580C | 2 |
EEF2 | STAD | chr19 | 3978014 | 3978014 | C | T | Missense_Mutation | p.A624T | 2 |
EEF2 | SKCM | chr19 | 3981385 | 3981385 | G | A | Silent | p.I321I | 2 |
EEF2 | BLCA | chr19 | 3984133 | 3984133 | C | G | Splice_Site | 2 | |
EEF2 | CESC | chr19 | 3984204 | 3984204 | G | A | Missense_Mutation | 2 | |
EEF2 | UCEC | chr19 | 3979984 | 3979984 | T | A | Missense_Mutation | p.D476V | 2 |
EEF2 | HNSC | chr19 | 3979393 | 3979393 | G | A | Silent | p.A549A | 1 |
EEF2 | LUAD | chr19 | 3984259 | 3984259 | G | A | Silent | p.G31G | 1 |
EEF2 | SKCM | chr19 | 3980661 | 3980661 | G | A | Silent | p.S399S | 1 |
EEF2 | ESCA | chr19 | 3982327 | 3982327 | G | A | Silent | p.F236 | 1 |
EEF2 | KIRP | chr19 | 3983291 | 3983293 | TGA | - | Splice_Site | p.T73_splice | 1 |
EEF2 | PRAD | chr19 | 3984159 | 3984159 | C | A | Nonsense_Mutation | p.E65* | 1 |
EEF2 | SKCM | chr19 | 3982416 | 3982416 | G | A | Missense_Mutation | p.P207S | 1 |
EEF2 | BLCA | chr19 | 3979971 | 3979971 | C | A | Silent | 1 | |
EEF2 | CESC | chr19 | 3977937 | 3977937 | G | A | Silent | p.I649I | 1 |
EEF2 | HNSC | chr19 | 3981953 | 3981954 | - | - | Frame_Shift_Ins | 1 | |
EEF2 | LIHC | chr19 | 3980657 | 3980657 | T | - | Frame_Shift_Del | p.M401fs | 1 |
EEF2 | HNSC | chr19 | 3977871 | 3977871 | G | A | Silent | p.Y671Y | 1 |
EEF2 | LUAD | chr19 | 3982316 | 3982316 | C | A | Missense_Mutation | p.G240V | 1 |
EEF2 | STAD | chr19 | 3979372 | 3979372 | G | A | Silent | 1 | |
EEF2 | ESCA | chr19 | 3982327 | 3982327 | G | A | Silent | p.F236F | 1 |
EEF2 | SKCM | chr19 | 3982904 | 3982904 | G | A | Silent | p.P171P | 1 |
EEF2 | BLCA | chr19 | 3977937 | 3977937 | G | C | Missense_Mutation | 1 | |
EEF2 | CESC | chr19 | 3977937 | 3977937 | G | A | Silent | p.I649 | 1 |
EEF2 | HNSC | chr19 | 3983151 | 3983151 | G | C | Silent | 1 | |
EEF2 | LIHC | chr19 | 3982351 | 3982351 | A | - | Frame_Shift_Del | p.F228fs | 1 |
EEF2 | HNSC | chr19 | 3980975 | 3980975 | A | G | Silent | p.A338A | 1 |
EEF2 | LUAD | chr19 | 3982312 | 3982312 | C | A | Missense_Mutation | p.E241D | 1 |
EEF2 | BLCA | chr19 | 3977937 | 3977937 | G | C | Missense_Mutation | p.I649M | 1 |
EEF2 | COAD | chr19 | 3982967 | 3982967 | G | A | Silent | p.R150R | 1 |
EEF2 | ESCA | chr19 | 3980008 | 3980008 | T | C | Missense_Mutation | 1 | |
EEF2 | KIRP | chr19 | 3983279 | 3983279 | G | T | Missense_Mutation | 1 | |
EEF2 | SARC | chr19 | 3977486 | 3977486 | A | G | Silent | 1 | |
EEF2 | STAD | chr19 | 3982258 | 3982260 | CTT | - | In_Frame_Del | p.259_260del | 1 |
EEF2 | SKCM | chr19 | 3984182 | 3984182 | G | A | Missense_Mutation | p.T57I | 1 |
EEF2 | BLCA | chr19 | 3979408 | 3979408 | A | G | Silent | 1 | |
EEF2 | CESC | chr19 | 3978083 | 3978083 | G | A | Missense_Mutation | p.R601W | 1 |
EEF2 | HNSC | chr19 | 3983263 | 3983263 | G | A | Missense_Mutation | 1 | |
EEF2 | LIHC | chr19 | 3984195 | 3984195 | C | - | Frame_Shift_Del | p.E53fs | 1 |
EEF2 | HNSC | chr19 | 3983259 | 3983259 | C | T | Silent | p.E83E | 1 |
EEF2 | BLCA | chr19 | 3983208 | 3983208 | G | T | Silent | p.I100I | 1 |
EEF2 | COAD | chr19 | 3984134 | 3984134 | G | A | Missense_Mutation | p.T73I | 1 |
EEF2 | ESCA | chr19 | 3984281 | 3984281 | A | G | Missense_Mutation | 1 | |
EEF2 | UCEC | chr19 | 3979938 | 3979938 | C | T | Silent | p.A491A | 1 |
EEF2 | GBM | chr19 | 3980665 | 3980665 | A | C | Missense_Mutation | p.I398S | 1 |
EEF2 | LGG | chr19 | 3980680 | 3980680 | G | T | Missense_Mutation | p.P393H | 1 |
EEF2 | SARC | chr19 | 3982897 | 3982897 | G | T | Missense_Mutation | 1 | |
EEF2 | STAD | chr19 | 3977575 | 3977575 | G | A | Missense_Mutation | p.R701C | 1 |
EEF2 | SKCM | chr19 | 3980662 | 3980662 | G | A | Missense_Mutation | p.S399F | 1 |
EEF2 | BLCA | chr19 | 3983208 | 3983208 | G | T | Silent | 1 | |
EEF2 | CESC | chr19 | 3984204 | 3984204 | G | A | Missense_Mutation | p.R50W | 1 |
EEF2 | HNSC | chr19 | 3983259 | 3983259 | C | T | Silent | 1 | |
EEF2 | LIHC | chr19 | 3982002 | 3982002 | G | - | Frame_Shift_Del | p.P280fs | 1 |
EEF2 | DLBC | chr19 | 3980852 | 3980852 | G | A | Silent | p.D379D | 1 |
EEF2 | BRCA | chr19 | 3983184 | 3983184 | A | G | Silent | p.H108 | 1 |
EEF2 | GBM | chr19 | 3977992 | 3977992 | C | T | Missense_Mutation | 1 | |
EEF2 | LGG | chr19 | 3980680 | 3980680 | G | T | Missense_Mutation | 1 | |
EEF2 | SKCM | chr19 | 3977471 | 3977471 | G | A | Silent | p.T735T | 1 |
EEF2 | STAD | chr19 | 3982258 | 3982260 | CTT | - | In_Frame_Del | p.259_260KL>T | 1 |
EEF2 | LUAD | chr19 | 3984142 | 3984142 | G | C | Missense_Mutation | p.I70M | 1 |
EEF2 | SKCM | chr19 | 3977564 | 3977564 | G | A | Silent | p.V704V | 1 |
EEF2 | BLCA | chr19 | 3982047 | 3982047 | G | A | Silent | 1 | |
EEF2 | CESC | chr19 | 3979965 | 3979965 | C | T | Silent | p.T482 | 1 |
EEF2 | HNSC | chr19 | 3976713 | 3976713 | C | A | Missense_Mutation | 1 | |
EEF2 | HNSC | chr19 | 3979344 | 3979344 | C | T | Missense_Mutation | p.A566T | 1 |
EEF2 | BLCA | chr19 | 3979977 | 3979977 | G | A | Silent | p.F478F | 1 |
EEF2 | GBM | chr19 | 3984284 | 3984284 | G | T | Missense_Mutation | 1 | |
EEF2 | LGG | chr19 | 3979890 | 3979890 | C | A | Silent | 1 | |
EEF2 | THYM | chr19 | 3984223 | 3984223 | C | T | Silent | 1 | |
EEF2 | LUAD | chr19 | 3983180 | 3983181 | - | A | Frame_Shift_Ins | p.L110fs | 1 |
EEF2 | SKCM | chr19 | 3977513 | 3977513 | G | A | Silent | p.I721I | 1 |
EEF2 | BLCA | chr19 | 3979977 | 3979977 | G | A | Silent | 1 | |
EEF2 | CESC | chr19 | 3984340 | 3984340 | G | A | Silent | p.F4 | 1 |
EEF2 | UCS | chr19 | 3979392 | 3979393 | - | GGCGCCCGCGATGATGT | Frame_Shift_Ins | p.G550fs | 1 |
EEF2 | HNSC | chr19 | 3977901 | 3977901 | G | A | Silent | 1 | |
EEF2 | HNSC | chr19 | 3981953 | 3981954 | - | G | Frame_Shift_Ins | p.L297fs | 1 |
EEF2 | PAAD | chr19 | 3976682 | 3976682 | T | A | Missense_Mutation | 1 | |
EEF2 | STAD | chr19 | 3979372 | 3979372 | G | A | Silent | p.I556I | 1 |
EEF2 | BLCA | chr19 | 3984165 | 3984165 | C | T | Missense_Mutation | p.E63K | 1 |
EEF2 | THYM | chr19 | 3977297 | 3977297 | G | A | Missense_Mutation | p.R767W | 1 |
EEF2 | CESC | chr19 | 3982020 | 3982020 | G | T | Missense_Mutation | 1 | |
EEF2 | GBM | chr19 | 3984325 | 3984325 | G | A | Silent | 1 | |
EEF2 | LIHC | chr19 | 3983227 | 3983227 | T | C | Missense_Mutation | 1 | |
EEF2 | HNSC | chr19 | 3979344 | 3979344 | C | T | Missense_Mutation | 1 | |
EEF2 | LUAD | chr19 | 3976626 | 3976626 | C | A | Missense_Mutation | p.V835L | 1 |
EEF2 | LUAD | chr19 | 3976626 | 3976627 | CC | AA | Missense_Mutation | p.V835L | 1 |
EEF2 | SKCM | chr19 | 3976654 | 3976654 | G | A | Silent | p.F825F | 1 |
EEF2 | BLCA | chr19 | 3984165 | 3984165 | C | T | Missense_Mutation | 1 | |
EEF2 | COAD | chr19 | 3976696 | 3976696 | C | T | Silent | p.Q811Q | 1 |
EEF2 | KIRC | chr19 | 3980044 | 3980044 | C | A | Missense_Mutation | p.R456L | 1 |
EEF2 | BLCA | chr19 | 3979840 | 3979840 | A | T | Missense_Mutation | p.L524Q | 1 |
EEF2 | CESC | chr19 | 3984340 | 3984340 | G | A | Silent | 1 | |
EEF2 | GBM | chr19 | 3980062 | 3980062 | G | T | Missense_Mutation | 1 | |
EEF2 | LIHC | chr19 | 3980669 | 3980669 | A | T | Missense_Mutation | 1 | |
EEF2 | HNSC | chr19 | 3979393 | 3979393 | G | A | Silent | 1 | |
EEF2 | LUAD | chr19 | 3976627 | 3976627 | C | A | Silent | p.V834V | 1 |
EEF2 | LUSC | chr19 | 3977846 | 3977846 | C | A | Missense_Mutation | p.V680L | 1 |
EEF2 | SKCM | chr19 | 3978042 | 3978042 | G | A | Silent | p.A614A | 1 |
EEF2 | BLCA | chr19 | 3979840 | 3979840 | A | T | Missense_Mutation | 1 | |
EEF2 | BLCA | chr19 | 3980668 | 3980668 | T | C | Missense_Mutation | p.Y397C | 1 |
EEF2 | ESCA | chr19 | 3982032 | 3982032 | G | A | Silent | p.N270 | 1 |
EEF2 | ESCA | chr19 | 3976744 | 3976744 | G | T | Silent | p.G795G | 1 |
EEF2 | PAAD | chr19 | 3977458 | 3977458 | G | T | Missense_Mutation | 1 | |
EEF2 | THYM | chr19 | 3976646 | 3976646 | C | T | Missense_Mutation | p.S828N | 1 |
EEF2 | GBM | chr19 | 3980665 | 3980665 | A | C | Missense_Mutation | 1 | |
EEF2 | LIHC | chr19 | 3981359 | 3981359 | T | G | Missense_Mutation | p.K330T | 1 |
EEF2 | HNSC | chr19 | 3983263 | 3983263 | G | A | Missense_Mutation | p.S82L | 1 |
EEF2 | LUAD | chr19 | 3984192 | 3984192 | T | A | Missense_Mutation | p.T54S | 1 |
EEF2 | LUSC | chr19 | 3980012 | 3980013 | CA | - | Frame_Shift_Del | p.C466fs | 1 |
EEF2 | SKCM | chr19 | 3978015 | 3978015 | G | A | Silent | p.S623S | 1 |
EEF2 | BLCA | chr19 | 3979425 | 3979425 | C | T | Missense_Mutation | 1 | |
EEF2 | COAD | chr19 | 3977916 | 3977916 | G | A | Silent | p.G656G | 1 |
EEF2 | BLCA | chr19 | 3984133 | 3984133 | C | G | Splice_Site | p.T73_splice | 1 |
EEF2 | ESCA | chr19 | 3984281 | 3984281 | A | G | Missense_Mutation | p.V24A | 1 |
EEF2 | PCPG | chr19 | 3978145 | 3978145 | C | T | Missense_Mutation | p.R580H | 1 |
EEF2 | SKCM | chr19 | 3979950 | 3979950 | G | A | Silent | p.T487T | 1 |
EEF2 | THYM | chr19 | 3984223 | 3984223 | C | T | Silent | p.A43A | 1 |
EEF2 | BLCA | chr19 | 3977234 | 3977234 | G | A | Silent | 1 | |
EEF2 | CESC | chr19 | 3982314 | 3982314 | C | - | Frame_Shift_Del | 1 | |
EEF2 | HNSC | chr19 | 3977871 | 3977871 | G | A | Silent | 1 | |
EEF2 | LIHC | chr19 | 3980917 | 3980917 | G | C | Missense_Mutation | p.L358V | 1 |
EEF2 | HNSC | chr19 | 3983151 | 3983151 | G | C | Silent | p.L119L | 1 |
EEF2 | LUAD | chr19 | 3983168 | 3983168 | C | A | Nonsense_Mutation | p.E114* | 1 |
EEF2 | SKCM | chr19 | 3982304 | 3982304 | A | G | Missense_Mutation | p.L244S | 1 |
EEF2 | BLCA | chr19 | 3980668 | 3980668 | T | C | Missense_Mutation | 1 | |
EEF2 | COAD | chr19 | 3979940 | 3979940 | C | T | Missense_Mutation | p.A491T | 1 |
EEF2 | ESCA | chr19 | 3978064 | 3978064 | C | A | Missense_Mutation | p.R607L | 1 |
EEF2 | KIRP | chr19 | 3983291 | 3983293 | TGA | - | Splice_Site | 1 | |
EEF2 | UCEC | chr19 | 3982300 | 3982300 | C | T | Silent | p.G245G | 1 |
EEF2 | HNSC | chr19 | 3982347 | 3982347 | C | T | Missense_Mutation | 1 | |
EEF2 | LIHC | chr19 | 3982287 | 3982287 | C | - | Frame_Shift_Del | p.A250fs | 1 |
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FusionGDB2 ID | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
103029 | N/A | AA452576 | AP2S1 | chr19 | 47341564 | + | EEF2 | chr19 | 3981413 | + |
103029 | N/A | AA706989 | AUP1 | chr2 | 74754188 | + | EEF2 | chr19 | 3981945 | + |
103029 | N/A | EC561306 | BCKDHB | chr6 | 80826093 | + | EEF2 | chr19 | 3977959 | + |
103029 | N/A | EC572773 | BRINP1 | chr9 | 121964314 | + | EEF2 | chr19 | 3979858 | + |
103029 | STAD | TCGA-CG-5721-01A | CCT4 | chr2 | 62104595 | - | EEF2 | chr19 | 3982053 | - |
96529 | N/A | T05979 | EEF2 | chr19 | 3976484 | + | ABHD6 | chr3 | 58223591 | + |
102890 | THCA | TCGA-EM-A1YA-01A | EEF2 | chr19 | 3976055 | - | ANKS1A | chr6 | 34977682 | + |
95236 | KIRP | TCGA-A4-A5Y1-01A | EEF2 | chr19 | 3976055 | - | ARFGEF2 | chr20 | 47615777 | + |
101628 | STAD | TCGA-BR-A4PD-01A | EEF2 | chr19 | 3976108 | - | B2M | chr15 | 45009809 | + |
97738 | LUAD | TCGA-86-A4D0-01A | EEF2 | chr19 | 3976055 | - | CBS | chr21 | 44476011 | - |
100476 | OV | TCGA-09-2056 | EEF2 | chr19 | 3977816 | - | CKS1B | chr1 | 154947117 | + |
98105 | HNSC | TCGA-BB-4223-01A | EEF2 | chr19 | 3976055 | - | CLCN3 | chr4 | 170623929 | + |
99855 | N/A | BC068002 | EEF2 | chr19 | 3979817 | - | CSNK1D | chr17 | 80206799 | - |
102507 | TGCT | TCGA-SB-A6J6-01A | EEF2 | chr19 | 3976055 | - | DDX21 | chr10 | 70723858 | + |
102756 | STAD | TCGA-BR-8589-01A | EEF2 | chr19 | 3976055 | - | DDX27 | chr20 | 47849303 | + |
98111 | SARC | TCGA-HB-A3YV-01A | EEF2 | chr19 | 3976055 | - | EEA1 | chr12 | 93229203 | - |
103029 | N/A | AI075687 | EEF2 | chr19 | 3982344 | + | EEF2 | chr19 | 3977241 | + |
103029 | N/A | BE173877 | EEF2 | chr19 | 3977925 | - | EEF2 | chr19 | 3982305 | - |
103029 | N/A | BE763496 | EEF2 | chr19 | 3980915 | + | EEF2 | chr19 | 3976336 | + |
103029 | N/A | BF761203 | EEF2 | chr19 | 3976742 | + | EEF2 | chr19 | 3980695 | - |
103029 | N/A | BF801948 | EEF2 | chr19 | 3978117 | - | EEF2 | chr19 | 3979344 | + |
103029 | N/A | BF927334 | EEF2 | chr19 | 3976340 | - | EEF2 | chr19 | 3984194 | - |
103029 | N/A | BG031663 | EEF2 | chr19 | 3976181 | + | EEF2 | chr19 | 3976433 | - |
103029 | N/A | BQ347823 | EEF2 | chr19 | 3976563 | - | EEF2 | chr19 | 3976441 | + |
103029 | N/A | BQ349979 | EEF2 | chr19 | 3980548 | + | EEF2 | chr19 | 3985461 | - |
103029 | N/A | CD580061 | EEF2 | chr19 | 3981383 | - | EEF2 | chr19 | 3982967 | - |
103029 | N/A | CN263823 | EEF2 | chr19 | 3976672 | + | EEF2 | chr19 | 3976591 | - |
103029 | N/A | EC450536 | EEF2 | chr19 | 3980048 | + | EEF2 | chr19 | 3980523 | - |
94732 | STAD | TCGA-BR-8679-01A | EEF2 | chr19 | 3976055 | - | EIF2AK2 | chr2 | 37342384 | - |
93482 | THCA | TCGA-ET-A3DR-01A | EEF2 | chr19 | 3976055 | - | ERBB3 | chr12 | 56492035 | + |
94051 | N/A | N93529 | EEF2 | chr19 | 3976177 | + | F10 | chr13 | 113803434 | - |
96636 | STAD | TCGA-BR-8680-01A | EEF2 | chr19 | 3976055 | - | FAR1 | chr11 | 13744912 | + |
101372 | N/A | EC555622 | EEF2 | chr19 | 3980022 | + | GALNTL6 | chr4 | 173722742 | + |
25266 | HNSC | TCGA-UF-A7JJ | EEF2 | chr19 | 3984205 | - | IGHG1 | chr14 | 106209405 | - |
25266 | HNSC | TCGA-UF-A7JJ | EEF2 | chr19 | 3984205 | - | IGHG1 | chr14 | 106237740 | - |
98118 | SARC | TCGA-KD-A5QU-01A | EEF2 | chr19 | 3976055 | - | LAMA4 | chr6 | 112507969 | - |
100140 | STAD | TCGA-CG-4301-01A | EEF2 | chr19 | 3972316 | - | LIPF | chr10 | 90424198 | + |
97185 | N/A | T19923 | EEF2 | chr19 | 3976585 | + | LNX2 | chr13 | 28179015 | - |
25266 | N/A | AW499012 | EEF2 | chr19 | 3982298 | - | LRRC4B | chr19 | 51037650 | - |
100470 | Non-Cancer | 235N | EEF2 | chr19 | 3985375 | - | MAP2K2 | chr19 | 4090706 | - |
99162 | N/A | AW021402 | EEF2 | chr19 | 3976057 | - | MEF2C-AS1 | chr5 | 88390023 | - |
98609 | N/A | BG060184 | EEF2 | chr19 | 3976054 | - | MFHAS1 | chr8 | 8643265 | - |
81580 | ACC | TCGA-OR-A5L8-01A | EEF2 | chr19 | 3979830 | - | NRXN2 | chr11 | 64416337 | - |
98284 | N/A | BQ308618 | EEF2 | chr19 | 3981364 | - | OSR2 | chr8 | 99961810 | + |
90662 | UVM | TCGA-V4-A9E7-01A | EEF2 | chr19 | 3972316 | - | PABPC1 | chr8 | 101734220 | - |
89496 | N/A | BI495206 | EEF2 | chr19 | 3976054 | - | PAPSS1 | chr4 | 108538387 | - |
96331 | N/A | AW874543 | EEF2 | chr19 | 3976308 | + | PEX14 | chr1 | 10690464 | - |
98134 | LUAD | TCGA-86-6851-01A | EEF2 | chr19 | 3976055 | - | PLEKHA5 | chr12 | 19441012 | + |
96928 | N/A | BU958708 | EEF2 | chr19 | 3976149 | - | PRMT3 | chr11 | 20530001 | + |
98139 | ACC | TCGA-OR-A5KT-01A | EEF2 | chr19 | 3976055 | - | SEC63 | chr6 | 108214782 | - |
60961 | GBM | TCGA-27-2524-01A | EEF2 | chr19 | 3979327 | - | SHD | chr19 | 4282867 | + |
98682 | KIRC | TCGA-CW-5581-01A | EEF2 | chr19 | 3976055 | - | SIAE | chr11 | 124543777 | - |
67087 | N/A | DA998089 | EEF2 | chr19 | 3984161 | - | SLC25A10 | chr17 | 79679488 | + |
82610 | PRAD | TCGA-EJ-A46G | EEF2 | chr19 | 3983108 | - | SLC25A23 | chr19 | 6436479 | - |
82610 | PRAD | TCGA-EJ-A46G-01A | EEF2 | chr19 | 3983108 | - | SLC25A23 | chr19 | 6436475 | - |
101736 | Non-Cancer | TCGA-K1-A3PO-11A | EEF2 | chr19 | 3982805 | - | SMARCA4 | chr19 | 11151983 | + |
102816 | N/A | CV392722 | EEF2 | chr19 | 3980943 | + | SPTBN1 | chr2 | 54687249 | - |
94171 | N/A | BI861553 | EEF2 | chr19 | 3976054 | - | SUN2 | chr22 | 39159588 | - |
98474 | N/A | AI905878 | EEF2 | chr19 | 3980927 | + | TAPBP | chr6 | 33272807 | + |
99016 | LUAD | TCGA-44-5644-01A | EEF2 | chr19 | 3976055 | - | THSD4 | chr15 | 72072881 | + |
94367 | N/A | CV351549 | EEF2 | chr19 | 3978077 | - | TRRAP | chr7 | 98602225 | + |
102742 | DLBC | TCGA-GS-A9TT-01A | EEF2 | chr19 | 3976055 | - | TYK2 | chr19 | 10491352 | - |
103029 | OV | TCGA-61-1728 | GNB2 | chr7 | 100275038 | + | EEF2 | chr19 | 3978170 | - |
103029 | N/A | BG059476 | GPC6 | chr13 | 94011252 | + | EEF2 | chr19 | 3976054 | + |
103029 | N/A | AA523503 | GRIK1 | chr21 | 30946173 | - | EEF2 | chr19 | 3976054 | + |
103029 | Non-Cancer | TCGA-IN-8462-11A | MED25 | chr19 | 50339202 | + | EEF2 | chr19 | 3976745 | - |
103029 | LGG | TCGA-DH-A66D | PAK6 | chr15 | 40531758 | + | EEF2 | chr19 | 3982056 | - |
103029 | THYM | TCGA-ZB-A965-01A | PLTP | chr20 | 44527399 | - | EEF2 | chr19 | 3985461 | - |
103029 | STAD | TCGA-BR-4292 | RPS5 | chr19 | 58905962 | + | EEF2 | chr19 | 3980707 | - |
103029 | PRAD | TCGA-EJ-7125-01A | SPON2 | chr4 | 1201668 | - | EEF2 | chr19 | 3984348 | - |
103029 | N/A | BG230879 | SUN2 | chr22 | 39159588 | + | EEF2 | chr19 | 3976054 | + |
103029 | PRAD | TCGA-CH-5763-01A | TGM4 | chr3 | 44945479 | + | EEF2 | chr19 | 3984348 | - |
103031 | PRAD | TCGA-EJ-5511-01A | ZNF827 | chr4 | 146682281 | - | EEF2 | chr19 | 3985461 | - |
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Cancer type | Translation factor | Coefficent | Hazard ratio | Wald test pval | Likelihool ratio pval | Logrank test pval | # samples |
THYM | EEF2 | 2.61592638904488 | 0.961618294454737 | 0.00352852241645781 | 0.00496229781705997 | 0.0022970543894486 | 121 |
LGG | EEF2 | 1.71829724412909 | 0.541333826133561 | 0.00467293255419296 | 0.00566450923680074 | 0.00473431463683783 | 525 |
LUAD | EEF2 | 0.733569455303711 | -0.309832995624665 | 0.0129117595777454 | 0.0126482298810866 | 0.0129797780188127 | 564 |
LUAD | EEF2 | 0.733569455303711 | -0.309832995624665 | 0.0129117595777454 | 0.0126482298810866 | 0.0129797780188127 | 564 |
PAAD | EEF2 | 1.86797229638269 | 0.624853509066425 | 0.0143591460240746 | 0.0112639703905914 | 0.0142905816478425 | 182 |
PAAD | EEF2 | 1.86797229638269 | 0.624853509066425 | 0.0143591460240746 | 0.0112639703905914 | 0.0142905816478425 | 182 |
COAD | EEF2 | 1.68867363544652 | 0.523943389697086 | 0.0168678754984475 | 0.0152974623659947 | 0.0167444072187299 | 315 |
COAD | EEF2 | 1.68867363544652 | 0.523943389697086 | 0.0168678754984475 | 0.0152974623659947 | 0.0167444072187299 | 315 |
LIHC | EEF2 | 0.705089620999105 | -0.349430362264637 | 0.0182230879990776 | 0.0188702147067013 | 0.0185886870552413 | 417 |
LIHC | EEF2 | 0.705089620999105 | -0.349430362264637 | 0.0182230879990776 | 0.0188702147067013 | 0.0185886870552413 | 417 |
LAML | EEF2 | 0.612397908871423 | -0.490373029849404 | 0.023705390307799 | 0.0238682283578351 | 0.0235911972159276 | 160 |
PCPG | EEF2 | 0.184290693633243 | -1.69124091133148 | 0.0314070001401926 | 0.0155931899925496 | 0.0353360200441583 | 185 |
PCPG | EEF2 | 0.184290693633243 | -1.69124091133148 | 0.0314070001401926 | 0.0155931899925496 | 0.0353360200441583 | 185 |
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Cancer type | Translation factor | pval | adj.p |
TGCT | EEF2 | 0.000395282502251396 | 0.011 |
KIRC | EEF2 | 0.0072361452805692 | 0.2 |
LGG | EEF2 | 0.0409689870332943 | 1 |
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Cancer type | Translation factor | pval | adj.p |
LGG | EEF2 | 0.0020959545831738 | 0.067 |
UCEC | EEF2 | 0.000340423630189767 | 0.011 |
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![]() (DrugBank Version 5.1.8 2021-05-08) |
UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
P13639 | DB03223 | Diphthamide | Small molecule | Experimental | |
P13639 | DB08348 | N~2~,N~2~-DIMETHYL-N~1~-(6-OXO-5,6-DIHYDROPHENANTHRIDIN-2-YL)GLYCINAMIDE | Small molecule | Experimental | |
P13639 | DB11823 | Esketamine | Inhibitor | Small molecule | Approved|Investigational |
P13639 | DB12688 | Moxetumomab Pasudotox | Inactivator | Biotech | Approved|Investigational |
P13639 | DB03223 | Diphthamide | |||
P13639 | DB08348 | N~2~,N~2~-DIMETHYL-N~1~-(6-OXO-5,6-DIHYDROPHENANTHRIDIN-2-YL)GLYCINAMIDE | |||
P13639 | DB11823 | Esketamine | Inhibitor | ||
P13639 | DB12688 | Moxetumomab Pasudotox | Inactivator |
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![]() (DisGeNet 4.0) |
Disease ID | Disease Name | # PubMeds | Disease source |
C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
C0007134 | Renal Cell Carcinoma | 1 | CTD_human |
C0029408 | Degenerative polyarthritis | 1 | CTD_human |
C0086743 | Osteoarthrosis Deformans | 1 | CTD_human |
C0205641 | Adenocarcinoma, Basal Cell | 1 | CTD_human |
C0205642 | Adenocarcinoma, Oxyphilic | 1 | CTD_human |
C0205643 | Carcinoma, Cribriform | 1 | CTD_human |
C0205644 | Carcinoma, Granular Cell | 1 | CTD_human |
C0205645 | Adenocarcinoma, Tubular | 1 | CTD_human |
C0242379 | Malignant neoplasm of lung | 1 | CTD_human |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | 1 | CTD_human |
C0678222 | Breast Carcinoma | 1 | CTD_human |
C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
C1266042 | Chromophobe Renal Cell Carcinoma | 1 | CTD_human |
C1266043 | Sarcomatoid Renal Cell Carcinoma | 1 | CTD_human |
C1266044 | Collecting Duct Carcinoma of the Kidney | 1 | CTD_human |
C1306837 | Papillary Renal Cell Carcinoma | 1 | CTD_human |
C1836395 | SPINOCEREBELLAR ATAXIA 26 | 1 | CTD_human;ORPHANET;UNIPROT |
C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |