Primary Site >> Pancreatic Cancer
Gene >> EPPK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615648 |
| Start | 143871036:143871036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782491999 |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Val740Met(p.V740M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615648 |
| Start | 143872955:143872955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299A>T |
| AA Mutation | p.Gln100Leu(p.Q100L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615648 |
| Start | 143869085:143869085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4169G>A |
| AA Mutation | p.Ser1390Asn(p.S1390N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615648 |
| Start | 143872910:143872910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.344C>A |
| AA Mutation | p.Ala115Asp(p.A115D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615648 |
| Start | 143868004:143868004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546164646 |
| CDS Mutation | c.5250C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615648 |
| Start | 143870842:143870842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781950648 |
| CDS Mutation | c.2412G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |