Primary Site >> Pancreatic Cancer
Gene >> HEATR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366582 |
| Start | 236576913:236576913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2792T>C |
| AA Mutation | p.Val931Ala(p.V931A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366582 |
| Start | 236585089:236585089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2177C>T |
| AA Mutation | p.Ala726Val(p.A726V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366582 |
| Start | 236586265:236586265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1903C>A |
| AA Mutation | p.Pro635Thr(p.P635T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366582 |
| Start | 236592583:236592583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1244C>A |
| AA Mutation | p.Ser415Tyr(p.S415Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366582 |
| Start | 236576326:236576326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2977C>T |
| AA Mutation | p.His993Tyr(p.H993Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366582 |
| Start | 236581295:236581295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2682T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |