Primary Site >> Stomach Cancer
Gene >> SEPT9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77488786:77488786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1184T>A |
| AA Mutation | p.Val395Asp(p.V395D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77402589:77402589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.607A>T |
| AA Mutation | p.Ser203Cys(p.S203C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77482314:77482314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Glu298Lys(p.E298K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77488824:77488824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771639743 |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Val408Ile(p.V408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77402254:77402254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764983438 |
| CDS Mutation | c.272G>A |
| AA Mutation | p.Arg91Gln(p.R91Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77482252:77482252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830G>A |
| AA Mutation | p.Gly277Asp(p.G277D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77487513:77487513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003C>T |
| AA Mutation | p.Arg335Cys(p.R335C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427177 |
| Start | 77497350:77497350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1609C>T |
| AA Mutation | p.Arg537Trp(p.R537W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427177 |
| Start | 77482241:77482241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751622773 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000427177 |
| Start | 77487518:77487518(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1011delC |
| AA Mutation | p.Lys338ArgfsTer19(p.K338Rfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |