Primary Site >> Pancreatic Cancer
Gene >> MEFV
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219596 |
| Start | 3243521:3243521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1966G>A |
| AA Mutation | p.Glu656Lys(p.E656K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219596 |
| Start | 3249561:3249561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144998416 |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219596 |
| Start | 3243394:3243394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2093A>G |
| AA Mutation | p.Glu698Gly(p.E698G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219596 |
| Start | 3249648:3249648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104895198 |
| CDS Mutation | c.1043G>A |
| AA Mutation | p.Arg348His(p.R348H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219596 |
| Start | 3243600:3243600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1887G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219596 |
| Start | 3243588:3243588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776315170 |
| CDS Mutation | c.1899G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |