Primary Site >> Liver Cancer
Gene >> PIKFYVE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208352765:208352765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5827G>T |
| AA Mutation | p.Gly1943Trp(p.G1943W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208352766:208352766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5828G>C |
| AA Mutation | p.Gly1943Ala(p.G1943A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208324145:208324145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2194A>G |
| AA Mutation | p.Arg732Gly(p.R732G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208302280:208302280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1247G>T |
| AA Mutation | p.Gly416Val(p.G416V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208276807:208276807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418G>C |
| AA Mutation | p.Glu140Gln(p.E140Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264380 |
| Start | 208320306:208320306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2137T>G |
| AA Mutation | p.Tyr713Asp(p.Y713D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208354017:208354017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774554872 |
| CDS Mutation | c.5964A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264380 |
| Start | 208330667:208330667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767932394 |
| CDS Mutation | c.3936A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |