Primary Site >> Stomach Cancer
Gene >> ASIC1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000447966 |
| Start | 50077363:50077363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.709G>A |
| AA Mutation | p.Asp237Asn(p.D237N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447966 |
| Start | 50078532:50078532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Arg317Cys(p.R317C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447966 |
| Start | 50058803:50058803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368761955 |
| CDS Mutation | c.37G>A |
| AA Mutation | p.Val13Ile(p.V13I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447966 |
| Start | 50058830:50058830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.64G>A |
| AA Mutation | p.Ala22Thr(p.A22T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447966 |
| Start | 50058781:50058781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773285015 |
| CDS Mutation | c.15C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000447966 |
| Start | 50059920:50059920(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.529delG |
| AA Mutation | p.Glu177ArgfsTer31(p.E177Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000447966 |
| Start | 50079914:50079916(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1066_1068delAAG |
| AA Mutation | p.Lys356del(p.K356del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |