Primary Site >> Stomach Cancer
Gene >> CYP2D6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42126678:42126678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1390T>G |
| AA Mutation | p.Phe464Val(p.F464V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42128897:42128897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.553G>A |
| AA Mutation | p.Val185Met(p.V185M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42127629:42127629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.991G>T |
| AA Mutation | p.Val331Phe(p.V331F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42127875:42127875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.952C>A |
| AA Mutation | p.Leu318Ile(p.L318I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42127545:42127545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79489631 |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Val359Met(p.V359M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000360608 |
| Start | 42127842:42127842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150216909 |
| CDS Mutation | c.985C>T |
| AA Mutation | p.Arg329Cys(p.R329C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42126925:42126925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574629217 |
| CDS Mutation | c.1241G>A |
| AA Mutation | p.Arg414His(p.R414H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42126944:42126944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200621644 |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Val408Ile(p.V408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360608 |
| Start | 42126579:42126579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370580423 |
| CDS Mutation | c.1489C>T |
| AA Mutation | p.Arg497Cys(p.R497C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |