Primary Site >> Liver Cancer
Gene >> PTPRH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55181783:55181783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201369294 |
| CDS Mutation | c.3319G>A |
| AA Mutation | p.Ala1107Thr(p.A1107T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55203925:55203925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743A>G |
| AA Mutation | p.Asp248Gly(p.D248G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55202140:55202140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1069G>C |
| AA Mutation | p.Glu357Gln(p.E357Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55205539:55205539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.406G>T |
| AA Mutation | p.Ala136Ser(p.A136S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376350 |
| Start | 55203822:55203822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767275886 |
| CDS Mutation | c.846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376350 |
| Start | 55203882:55203882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |