Primary Site >> Stomach Cancer
Gene >> ACTA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432171:229432171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631G>A |
| AA Mutation | p.Val211Met(p.V211M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432294:229432294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Cys(p.R198C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432556:229432556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Gly152Ser(p.G152S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366684 |
| Start | 229431794:229431794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.917C>T |
| AA Mutation | p.Thr306Met(p.T306M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432409:229432409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757701835 |
| CDS Mutation | c.477C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432394:229432394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.492C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432064:229432064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748592740 |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366684 |
| Start | 229432575:229432575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371410845 |
| CDS Mutation | c.435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |