Primary Site >> Pancreatic Cancer
Gene >> PRKDC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314191 |
| Start | 47778794:47778794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11585C>T |
| AA Mutation | p.Ala3862Val(p.A3862V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314191 |
| Start | 47778795:47778795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568709506 |
| CDS Mutation | c.11584G>A |
| AA Mutation | p.Ala3862Thr(p.A3862T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314191 |
| Start | 47830687:47830687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8315A>G |
| AA Mutation | p.Tyr2772Cys(p.Y2772C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314191 |
| Start | 47877806:47877806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5281T>G |
| AA Mutation | p.Leu1761Val(p.L1761V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314191 |
| Start | 47778622:47778622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11690T>G |
| AA Mutation | p.Phe3897Cys(p.F3897C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314191 |
| Start | 47831897:47831897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8182C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |