Primary Site >> Stomach Cancer
Gene >> MAOA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338702 |
| Start | 43744415:43744415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1486C>T |
| AA Mutation | p.Pro496Ser(p.P496S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338702 |
| Start | 43731280:43731280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.685C>T |
| AA Mutation | p.Arg229Trp(p.R229W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338702 |
| Start | 43744485:43744485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1556A>T |
| AA Mutation | p.Tyr519Phe(p.Y519F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338702 |
| Start | 43744135:43744135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762042526 |
| CDS Mutation | c.1401C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338702 |
| Start | 43728273:43728273(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.608delG |
| AA Mutation | p.Gly203AlafsTer18(p.G203Afs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000338702 |
| Start | 43731825:43731825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.927T>G |
| AA Mutation | p.Tyr309Ter(p.Y309*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338702 |
| Start | 43693424:43693425(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.303_306dupCAAG |
| AA Mutation | p.Gly103GlnfsTer25(p.G103Qfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |