Primary Site >> Liver Cancer
Gene >> RIPK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216274 |
| Start | 24337705:24337705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.890C>T |
| AA Mutation | p.Ala297Val(p.A297V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216274 |
| Start | 24339482:24339482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571257852 |
| CDS Mutation | c.136G>A |
| AA Mutation | p.Asp46Asn(p.D46N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216274 |
| Start | 24339223:24339223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.263C>T |
| AA Mutation | p.Pro88Leu(p.P88L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216274 |
| Start | 24337344:24337344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1017T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216274 |
| Start | 24338033:24338033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.672C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000216274 |
| Start | 24336393:24336393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186368014 |
| CDS Mutation | c.1339C>T |
| AA Mutation | p.Arg447Ter(p.R447*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |