Primary Site >> Esophagus Cancer
Gene >> F8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929733:154929733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4057G>A |
| AA Mutation | p.Asp1353Asn(p.D1353N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930417:154930417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3373G>C |
| AA Mutation | p.Ala1125Pro(p.A1125P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154966633:154966633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146581224 |
| CDS Mutation | c.1064G>A |
| AA Mutation | p.Arg355Gln(p.R355Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929842:154929842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3948A>G |
| AA Mutation | p.Ile1316Met(p.I1316M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930397:154930397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3393T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930610:154930610(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3180delA |
| AA Mutation | p.Val1061Ter(p.V1061*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |