Primary Site >> Pancreatic Cancer
Gene >> CACNA1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181651405:181651405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1019T>A |
| AA Mutation | p.Phe340Tyr(p.F340Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181733019:181733019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2933C>A |
| AA Mutation | p.Ala978Asp(p.A978D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181763505:181763505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4789C>A |
| AA Mutation | p.Leu1597Met(p.L1597M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181793770:181793770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6004C>T |
| AA Mutation | p.Pro2002Ser(p.P2002S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181721803:181721803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2002C>T |
| AA Mutation | p.Arg668Cys(p.R668C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181772216:181772216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5124C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798756:181798756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768838447 |
| CDS Mutation | c.6864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |