Primary Site >> Stomach Cancer
Gene >> SULT1A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314752 |
| Start | 28606847:28606847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771144668 |
| CDS Mutation | c.508G>A |
| AA Mutation | p.Gly170Arg(p.G170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314752 |
| Start | 28607056:28607056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138013613 |
| CDS Mutation | c.394G>A |
| AA Mutation | p.Ala132Thr(p.A132T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314752 |
| Start | 28608567:28608567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185A>G |
| AA Mutation | p.Tyr62Cys(p.Y62C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314752 |
| Start | 28608361:28608361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302C>G |
| AA Mutation | p.Ala101Gly(p.A101G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314752 |
| Start | 28608827:28608827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.29C>T |
| AA Mutation | p.Pro10Leu(p.P10L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314752 |
| Start | 28608838:28608838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314752 |
| Start | 28605851:28605851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.858C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314752 |
| Start | 28607057:28607057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143774918 |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314752 |
| Start | 28608787:28608799(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.57_69delGCTCATCAAGTAC |
| AA Mutation | p.Ile21GlnfsTer30(p.I21Qfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |