Primary Site >> Stomach Cancer
Gene >> ETV1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405218 |
| Start | 13909659:13909659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.913A>C |
| AA Mutation | p.Thr305Pro(p.T305P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405218 |
| Start | 13988104:13988104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115C>A |
| AA Mutation | p.Leu39Met(p.L39M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405218 |
| Start | 13931666:13931666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748182764 |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213His(p.R213H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405218 |
| Start | 13931533:13931533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.771A>C |
| AA Mutation | p.Lys257Asn(p.K257N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405218 |
| Start | 13906577:13906577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.963A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405218 |
| Start | 13931665:13931665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.639C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405218 |
| Start | 13931716:13931716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.588C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405218 |
| Start | 13935848:13935848(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.414delC |
| AA Mutation | p.Thr139HisfsTer116(p.T139Hfs*116) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000405218 |
| Start | 13911239:13911239(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.871delG |
| AA Mutation | p.Gly291AlafsTer52(p.G291Afs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000405218 |
| Start | 13935847:13935848(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769886672 |
| CDS Mutation | c.414dupC |
| AA Mutation | p.Thr139HisfsTer24(p.T139Hfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |