Primary Site >> Pancreatic Cancer
Gene >> FANCM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267430 |
| Start | 45189126:45189126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5104G>T |
| AA Mutation | p.Asp1702Tyr(p.D1702Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267430 |
| Start | 45167013:45167013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1852G>C |
| AA Mutation | p.Val618Leu(p.V618L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267430 |
| Start | 45176049:45176049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767815301 |
| CDS Mutation | c.3295C>T |
| AA Mutation | p.Arg1099Cys(p.R1099C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267430 |
| Start | 45189358:45189358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5336A>C |
| AA Mutation | p.Gln1779Pro(p.Q1779P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267430 |
| Start | 45136200:45136200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.169T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267430 |
| Start | 45198750:45198750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766031579 |
| CDS Mutation | c.5823C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |