Primary Site >> Liver Cancer
Gene >> PRKG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 51804672:51804672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.635A>G |
| AA Mutation | p.Tyr212Cys(p.Y212C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 52282255:52282255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1603C>T |
| AA Mutation | p.His535Tyr(p.H535Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 52282292:52282292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1640T>C |
| AA Mutation | p.Leu547Pro(p.L547P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 52271434:52271434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213C>T |
| AA Mutation | p.His405Tyr(p.H405Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 52062601:52062601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.860G>T |
| AA Mutation | p.Gly287Val(p.G287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373985 |
| Start | 51467825:51467825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.536C>T |
| AA Mutation | p.Ala179Val(p.A179V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373985 |
| Start | 52288841:52288841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541150590 |
| CDS Mutation | c.1780C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373985 |
| Start | 52062602:52062602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.861A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |