Primary Site >> Stomach Cancer
Gene >> ELMO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37213358:37213358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.931A>G |
| AA Mutation | p.Thr311Ala(p.T311A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37225011:37225011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.569A>T |
| AA Mutation | p.Lys190Met(p.K190M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37225011:37225011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.569A>C |
| AA Mutation | p.Lys190Thr(p.K190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37224982:37224982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751048183 |
| CDS Mutation | c.598C>T |
| AA Mutation | p.Arg200Trp(p.R200W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310758 |
| Start | 37096619:37096619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1300C>T |
| AA Mutation | p.Pro434Ser(p.P434S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37133206:37133206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748062510 |
| CDS Mutation | c.1115C>T |
| AA Mutation | p.Thr372Met(p.T372M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37259206:37259206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388A>C |
| AA Mutation | p.Thr130Pro(p.T130P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 36894965:36894965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1490G>C |
| AA Mutation | p.Ser497Thr(p.S497T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37133147:37133147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1174C>A |
| AA Mutation | p.Gln392Lys(p.Q392K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37233175:37233175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469T>C |
| AA Mutation | p.Phe157Leu(p.F157L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310758 |
| Start | 37244389:37244389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416G>A |
| AA Mutation | p.Arg139Gln(p.R139Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 36861682:36861682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1960T>G |
| AA Mutation | p.Phe654Val(p.F654V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310758 |
| Start | 37213336:37213336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953A>G |
| AA Mutation | p.Gln318Arg(p.Q318R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37224921:37224921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776057144 |
| CDS Mutation | c.659C>T |
| AA Mutation | p.Ala220Val(p.A220V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310758 |
| Start | 36870475:36870475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1823T>G |
| AA Mutation | p.Leu608Arg(p.L608R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37314867:37314867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.175T>G |
| AA Mutation | p.Phe59Val(p.F59V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 36887620:36887620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1654C>T |
| AA Mutation | p.Arg552Cys(p.R552C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37314876:37314876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166A>G |
| AA Mutation | p.Ser56Gly(p.S56G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 36870472:36870472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751395548 |
| CDS Mutation | c.1826C>T |
| AA Mutation | p.Pro609Leu(p.P609L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37096678:37096678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241G>A |
| AA Mutation | p.Gly414Asp(p.G414D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310758 |
| Start | 37213417:37213417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778770532 |
| CDS Mutation | c.872C>T |
| AA Mutation | p.Ala291Val(p.A291V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 37013329:37013329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1407A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 37259249:37259249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770798452 |
| CDS Mutation | c.345G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 37233107:37233107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150348909 |
| CDS Mutation | c.537G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 36878056:36878056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766085000 |
| CDS Mutation | c.1776A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 37211440:37211440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310758 |
| Start | 36855602:36855602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377709624 |
| CDS Mutation | c.2133G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310758 |
| Start | 37271863:37271863(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.212delA |
| AA Mutation | p.Asn71MetfsTer7(p.N71Mfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310758 |
| Start | 37096695:37096696(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1223dupA |
| AA Mutation | p.His409AlafsTer2(p.H409Afs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310758 |
| Start | 37315954:37315955(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs766966664 |
| CDS Mutation | c.84dupA |
| AA Mutation | p.Pro29ThrfsTer11(p.P29Tfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |