Primary Site >> Stomach Cancer
Gene >> ETV7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340181 |
| Start | 36371465:36371465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529C>A |
| AA Mutation | p.Pro177Thr(p.P177T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340181 |
| Start | 36366954:36366954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370083197 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Glu277Lys(p.E277K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340181 |
| Start | 36375922:36375922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs9394345 |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Ala86Thr(p.A86T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340181 |
| Start | 36375886:36375886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775769716 |
| CDS Mutation | c.292C>T |
| AA Mutation | p.Arg98Cys(p.R98C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340181 |
| Start | 36371478:36371478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751876214 |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000340181 |
| Start | 36368938:36368939(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.797dupG |
| AA Mutation | p.Asn267LysfsTer22(p.N267Kfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |