Primary Site >> Pancreatic Cancer
Gene >> CACNA1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13214300:13214300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5873C>A |
| AA Mutation | p.Ala1958Asp(p.A1958D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13259586:13259586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4366T>C |
| AA Mutation | p.Ser1456Pro(p.S1456P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13299204:13299204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2429A>G |
| AA Mutation | p.His810Arg(p.H810R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000360228 |
| Start | 13308249:13308249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1784A>G |
| AA Mutation | p.Tyr595Cys(p.Y595C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13298951:13298951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2682G>T |
| AA Mutation | p.Glu894Asp(p.E894D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13334439:13334439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1137G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13235004:13235004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200501726 |
| CDS Mutation | c.5166C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13286523:13286524(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs777609072 |
| CDS Mutation | c.3532dupC |
| AA Mutation | p.Leu1178ProfsTer38(p.L1178Pfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |