Primary Site >> Pancreatic Cancer
Gene >> PTPRF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591242:43591242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373662568 |
| CDS Mutation | c.1220G>A |
| AA Mutation | p.Arg407His(p.R407H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43619565:43619565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4924G>A |
| AA Mutation | p.Glu1642Lys(p.E1642K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43588866:43588866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.815T>C |
| AA Mutation | p.Leu272Pro(p.L272P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591093:43591093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779067201 |
| CDS Mutation | c.1071G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43605366:43605366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149446507 |
| CDS Mutation | c.3312G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43598820:43598820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2220G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |