Primary Site >> Stomach Cancer
Gene >> EPB41L3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5419827:5419827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1390T>G |
| AA Mutation | p.Leu464Val(p.L464V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416275:5416275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1610G>T |
| AA Mutation | p.Cys537Phe(p.C537F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397410:5397410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771374021 |
| CDS Mutation | c.2489C>T |
| AA Mutation | p.Thr830Met(p.T830M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5410607:5410607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143942399 |
| CDS Mutation | c.2080C>T |
| AA Mutation | p.Arg694Cys(p.R694C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5419779:5419779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780187679 |
| CDS Mutation | c.1438G>A |
| AA Mutation | p.Glu480Lys(p.E480K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5445197:5445197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.429G>T |
| AA Mutation | p.Leu143Phe(p.L143F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397250:5397250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2649G>T |
| AA Mutation | p.Gln883His(p.Q883H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5443868:5443868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.499C>A |
| AA Mutation | p.Pro167Thr(p.P167T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416288:5416288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1597A>G |
| AA Mutation | p.Lys533Glu(p.K533E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5419835:5419835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382A>G |
| AA Mutation | p.Gln461Arg(p.Q461R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5489162:5489162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.22G>T |
| AA Mutation | p.Asp8Tyr(p.D8Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5395111:5395111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3109A>G |
| AA Mutation | p.Lys1037Glu(p.K1037E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416216:5416216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1669G>C |
| AA Mutation | p.Asp557His(p.D557H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5394710:5394710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3237G>T |
| AA Mutation | p.Glu1079Asp(p.E1079D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5428402:5428402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.976C>T |
| AA Mutation | p.Arg326Trp(p.R326W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5434087:5434087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775170222 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Val214Met(p.V214M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000341928 |
| Start | 5396201:5396201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2973G>T |
| AA Mutation | p.Gln991His(p.Q991H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397404:5397404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2495C>T |
| AA Mutation | p.Ser832Phe(p.S832F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5394734:5394734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3213A>T |
| AA Mutation | p.Lys1071Asn(p.K1071N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5489119:5489119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Ala22Val(p.A22V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5419801:5419801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1416G>C |
| AA Mutation | p.Lys472Asn(p.K472N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5423438:5423438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1279G>T |
| AA Mutation | p.Ala427Ser(p.A427S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397389:5397389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143141379 |
| CDS Mutation | c.2510C>T |
| AA Mutation | p.Thr837Met(p.T837M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5394734:5394734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3213A>C |
| AA Mutation | p.Lys1071Asn(p.K1071N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397281:5397281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758061983 |
| CDS Mutation | c.2618C>T |
| AA Mutation | p.Ser873Leu(p.S873L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5398079:5398079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745916851 |
| CDS Mutation | c.2414C>T |
| AA Mutation | p.Ala805Val(p.A805V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5434012:5434012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Asp239Asn(p.D239N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5424308:5424308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1117G>T |
| AA Mutation | p.Ala373Ser(p.A373S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5394765:5394765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3182A>G |
| AA Mutation | p.Lys1061Arg(p.K1061R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397202:5397202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2697G>T |
| AA Mutation | p.Glu899Asp(p.E899D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5433966:5433966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.761G>A |
| AA Mutation | p.Arg254His(p.R254H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5438046:5438046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.594A>T |
| AA Mutation | p.Glu198Asp(p.E198D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397267:5397267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140662824 |
| CDS Mutation | c.2632G>A |
| AA Mutation | p.Gly878Arg(p.G878R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416300:5416300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150384501 |
| CDS Mutation | c.1585C>T |
| AA Mutation | p.Arg529Cys(p.R529C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000341928 |
| Start | 5407701:5407701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2157G>T |
| AA Mutation | p.Gln719His(p.Q719H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5415872:5415872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375430348 |
| CDS Mutation | c.2013G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5406840:5406840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2286C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397139:5397139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192974284 |
| CDS Mutation | c.2760C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5428379:5428379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.999C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5398078:5398078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2415G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5415968:5415968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1917C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5415929:5415929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186596462 |
| CDS Mutation | c.1956C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5489082:5489082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5398039:5398039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2454T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416253:5416253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201925314 |
| CDS Mutation | c.1632G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397409:5397409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747043897 |
| CDS Mutation | c.2490G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5489034:5489034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770581819 |
| CDS Mutation | c.150C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397304:5397304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2595C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5396324:5396324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779573005 |
| CDS Mutation | c.2850G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341928 |
| Start | 5397322:5397322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2577G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341928 |
| Start | 5416319:5416319(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1566delC |
| AA Mutation | p.Thr523HisfsTer44(p.T523Hfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341928 |
| Start | 5433505:5433505(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.876delA |
| AA Mutation | p.Lys292AsnfsTer7(p.K292Nfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341928 |
| Start | 5443848:5443848(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.519delA |
| AA Mutation | p.Lys173AsnfsTer14(p.K173Nfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341928 |
| Start | 5406837:5406837(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2289delC |
| AA Mutation | p.Val764CysfsTer12(p.V764Cfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000341928 |
| Start | 5397123:5397123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2776C>T |
| AA Mutation | p.Arg926Ter(p.R926*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000341928 |
| Start | 5398077:5398077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781377051 |
| CDS Mutation | c.2416C>T |
| AA Mutation | p.Arg806Ter(p.R806*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341928 |
| Start | 5478304:5478305(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.317dupA |
| AA Mutation | p.Pro107AlafsTer2(p.P107Afs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |