Primary Site >> Stomach Cancer
Gene >> TRPV1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3572134:3572134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2219G>C |
| AA Mutation | p.Arg740Pro(p.R740P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3580515:3580515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1489C>A |
| AA Mutation | p.Leu497Met(p.L497M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3591291:3591291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.347G>A |
| AA Mutation | p.Arg116Lys(p.R116K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3590359:3590359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759486588 |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213His(p.R213H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3571542:3571542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2329T>C |
| AA Mutation | p.Ser777Pro(p.S777P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3591324:3591324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.314G>A |
| AA Mutation | p.Ser105Asn(p.S105N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3591348:3591348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.290T>C |
| AA Mutation | p.Leu97Pro(p.L97P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399756 |
| Start | 3585889:3585889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200427518 |
| CDS Mutation | c.1262G>A |
| AA Mutation | p.Arg421Gln(p.R421Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399756 |
| Start | 3566857:3566857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752057134 |
| CDS Mutation | c.2478C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |