Primary Site >> Pancreatic Cancer
Gene >> ANK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347528 |
| Start | 41696688:41696688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146518198 |
| CDS Mutation | c.2723C>T |
| AA Mutation | p.Pro908Leu(p.P908L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347528 |
| Start | 41655750:41655750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5623C>T |
| AA Mutation | p.His1875Tyr(p.H1875Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347528 |
| Start | 41706185:41706185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2055T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347528 |
| Start | 41715059:41715059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347528 |
| Start | 41704089:41704089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2247C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347528 |
| Start | 41714207:41714207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1749C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |