Primary Site >> Pancreatic Cancer
Gene >> FRY
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542859 |
| Start | 32209650:32209650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4341A>T |
| AA Mutation | p.Lys1447Asn(p.K1447N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542859 |
| Start | 32209720:32209720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4411C>A |
| AA Mutation | p.Leu1471Ile(p.L1471I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542859 |
| Start | 32185118:32185118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776944889 |
| CDS Mutation | c.3289A>G |
| AA Mutation | p.Met1097Val(p.M1097V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542859 |
| Start | 32276493:32276493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8316C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542859 |
| Start | 32147866:32147866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199638995 |
| CDS Mutation | c.1311T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542859 |
| Start | 32194226:32194226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542859 |
| Start | 32278539:32278539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554801796 |
| CDS Mutation | c.8460C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |