Primary Site >> Stomach Cancer
Gene >> SMPD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6394005:6394005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1450G>A |
| AA Mutation | p.Ala484Thr(p.A484T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391753:6391753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.688C>T |
| AA Mutation | p.Arg230Cys(p.R230C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391772:6391772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747630243 |
| CDS Mutation | c.707C>T |
| AA Mutation | p.Pro236Leu(p.P236L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391402:6391402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140202512 |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Arg113Cys(p.R113C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6393257:6393257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559088058 |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378His(p.R378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6394330:6394330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619G>T |
| AA Mutation | p.Arg540Met(p.R540M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391966:6391966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2723669 |
| CDS Mutation | c.901G>A |
| AA Mutation | p.Val301Ile(p.V301I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391711:6391711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342245 |
| Start | 6394448:6394448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1737C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342245 |
| Start | 6391806:6391806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762102363 |
| CDS Mutation | c.741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342245 |
| Start | 6392056:6392056(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772960412 |
| CDS Mutation | c.996delC |
| AA Mutation | p.Phe333SerfsTer52(p.F333Sfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |