Primary Site >> Stomach Cancer
Gene >> NR1H3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441012 |
| Start | 47261375:47261375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182303471 |
| CDS Mutation | c.634G>T |
| AA Mutation | p.Gly212Cys(p.G212C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441012 |
| Start | 47268329:47268329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171G>A |
| AA Mutation | p.Ala391Thr(p.A391T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441012 |
| Start | 47260546:47260546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Cys(p.R124C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441012 |
| Start | 47261421:47261421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779302187 |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227His(p.R227H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441012 |
| Start | 47268609:47268609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441012 |
| Start | 47261693:47261693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |