Primary Site >> Pancreatic Cancer
Gene >> DYNC1H1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 101980440:101980440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774677904 |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Ala284Val(p.A284V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 101986687:101986687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2462C>T |
| AA Mutation | p.Ala821Val(p.A821V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 102005997:102005997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5543C>A |
| AA Mutation | p.Pro1848His(p.P1848H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 102027500:102027500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9004T>C |
| AA Mutation | p.Ser3002Pro(p.S3002P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 102027509:102027509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9013C>A |
| AA Mutation | p.Leu3005Met(p.L3005M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360184 |
| Start | 102039181:102039181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11387C>A |
| AA Mutation | p.Thr3796Asn(p.T3796N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360184 |
| Start | 102027424:102027424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs8010870 |
| CDS Mutation | c.8928A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360184 |
| Start | 102015897:102015897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762065704 |
| CDS Mutation | c.7284G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360184 |
| Start | 102048648:102048648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1127284 |
| CDS Mutation | c.13351C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |