Primary Site >> Stomach Cancer
Gene >> SASH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367467 |
| Start | 148532838:148532838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761124936 |
| CDS Mutation | c.1606C>T |
| AA Mutation | p.Arg536Trp(p.R536W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367467 |
| Start | 148532850:148532850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1618A>G |
| AA Mutation | p.Lys540Glu(p.K540E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367467 |
| Start | 148471465:148471465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575597604 |
| CDS Mutation | c.476G>A |
| AA Mutation | p.Arg159Gln(p.R159Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367467 |
| Start | 148548515:148548515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3701C>T |
| AA Mutation | p.Ala1234Val(p.A1234V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367467 |
| Start | 148519624:148519624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Pro314Ser(p.P314S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148440363:148440363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534691257 |
| CDS Mutation | c.342G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148527536:148527536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148531561:148531561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150728102 |
| CDS Mutation | c.1464G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544518:148544518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3048G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148532885:148532885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772449697 |
| CDS Mutation | c.1653C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148390211:148390211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768459233 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544293:148544293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565128259 |
| CDS Mutation | c.2823C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148519596:148519596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111245321 |
| CDS Mutation | c.912C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544749:148544749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3279A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148533869:148533869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759409120 |
| CDS Mutation | c.1833C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544569:148544569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776342522 |
| CDS Mutation | c.3099C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367467 |
| Start | 148487700:148487700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544240:148544240(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2774delC |
| AA Mutation | p.Pro925LeufsTer19(p.P925Lfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367467 |
| Start | 148527567:148527567(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1404delA |
| AA Mutation | p.Lys468AsnfsTer41(p.K468Nfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367467 |
| Start | 148544642:148544642(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761606832 |
| CDS Mutation | c.3177delC |
| AA Mutation | p.Trp1060GlyfsTer16(p.W1060Gfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367467 |
| Start | 148519714:148519715(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1036dupG |
| AA Mutation | p.Ala346GlyfsTer19(p.A346Gfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |