Primary Site >> Stomach Cancer
Gene >> SCRT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333291:144333291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941C>T |
| AA Mutation | p.Ala314Val(p.A314V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333519:144333519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713C>T |
| AA Mutation | p.Ala238Val(p.A238V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333631:144333631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.601G>A |
| AA Mutation | p.Ala201Thr(p.A201T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333426:144333426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806C>T |
| AA Mutation | p.Ser269Leu(p.S269L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144336135:144336135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.35T>G |
| AA Mutation | p.Leu12Arg(p.L12R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333355:144333355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Ala293Thr(p.A293T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333353:144333353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569446 |
| Start | 144333551:144333551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.681C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569446 |
| Start | 144336071:144336071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142851592 |
| CDS Mutation | c.99G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |