Primary Site >> Pancreatic Cancer
Gene >> DLC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13088629:13088629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778397065 |
| CDS Mutation | c.4150C>T |
| AA Mutation | p.Arg1384Cys(p.R1384C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13099585:13099585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2752C>T |
| AA Mutation | p.Arg918Trp(p.R918W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13100313:13100313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2024A>G |
| AA Mutation | p.Lys675Arg(p.K675R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276297 |
| Start | 13100410:13100410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1927C>T |
| AA Mutation | p.Pro643Ser(p.P643S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276297 |
| Start | 13110749:13110749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1495C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276297 |
| Start | 13100279:13100279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372344109 |
| CDS Mutation | c.2058G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |