Primary Site >> Esophagus Cancer
Gene >> DLC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13099546:13099546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2791G>A |
| AA Mutation | p.Gly931Arg(p.G931R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13499526:13499526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.546A>C |
| AA Mutation | p.Lys182Asn(p.K182N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13499055:13499055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1017G>T |
| AA Mutation | p.Lys339Asn(p.K339N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13088644:13088644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4135G>C |
| AA Mutation | p.Glu1379Gln(p.E1379Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13100058:13100058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144923726 |
| CDS Mutation | c.2279C>T |
| AA Mutation | p.Thr760Met(p.T760M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276297 |
| Start | 13115626:13115626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1380A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276297 |
| Start | 13088498:13088498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs73552359 |
| CDS Mutation | c.4281C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000276297 |
| Start | 13500021:13500021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.51G>A |
| AA Mutation | p.Trp17Ter(p.W17*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |