Primary Site >> Pancreatic Cancer
Gene >> BRD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15254239:15254239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774596084 |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Gly691Ser(p.G691S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15264636:15264636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.980C>T |
| AA Mutation | p.Pro327Leu(p.P327L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263377 |
| Start | 15273071:15273071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.29G>T |
| AA Mutation | p.Arg10Ile(p.R10I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15239178:15239178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3663C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15254159:15254159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200329089 |
| CDS Mutation | c.2151C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263377 |
| Start | 15255358:15255358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1986C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |