Primary Site >> Liver Cancer
Gene >> HHIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296575 |
| Start | 144658808:144658808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149715142 |
| CDS Mutation | c.491C>T |
| AA Mutation | p.Ala164Val(p.A164V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296575 |
| Start | 144659723:144659723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200798148 |
| CDS Mutation | c.716C>T |
| AA Mutation | p.Ser239Leu(p.S239L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296575 |
| Start | 144706634:144706634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935T>C |
| AA Mutation | p.Ile312Thr(p.I312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296575 |
| Start | 144646772:144646772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199961348 |
| CDS Mutation | c.97G>A |
| AA Mutation | p.Gly33Arg(p.G33R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296575 |
| Start | 144646799:144646799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.124G>T |
| AA Mutation | p.Gly42Trp(p.G42W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296575 |
| Start | 144659769:144659769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.762T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |