Primary Site >> Stomach Cancer
Gene >> TAF15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35844548:35844548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554593706 |
| CDS Mutation | c.1249G>A |
| AA Mutation | p.Gly417Ser(p.G417S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35844749:35844749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1450G>T |
| AA Mutation | p.Gly484Cys(p.G484C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35820186:35820186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141034613 |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Thr41Met(p.T41M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35842453:35842453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1000C>T |
| AA Mutation | p.Arg334Trp(p.R334W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35846929:35846929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776503828 |
| CDS Mutation | c.1763G>A |
| AA Mutation | p.Arg588His(p.R588H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605844 |
| Start | 35833918:35833918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.617G>A |
| AA Mutation | p.Arg206His(p.R206H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605844 |
| Start | 35844901:35844901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1602C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000605844 |
| Start | 35844882:35844882(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1589delG |
| AA Mutation | p.Gly530AlafsTer116(p.G530Afs*116) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000605844 |
| Start | 35844767:35844767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Arg490Ter(p.R490*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000605844 |
| Start | 35844854:35844854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1555C>T |
| AA Mutation | p.Arg519Ter(p.R519*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000605844 |
| Start | 35844881:35844882(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1588_1589dupGG |
| AA Mutation | p.Tyr531AlafsTer116(p.Y531Afs*116) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000605844 |
| Start | 35846904:35846904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1740-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |