Primary Site >> Stomach Cancer
Gene >> NR0B2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254227 |
| Start | 26911906:26911906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756121300 |
| CDS Mutation | c.713G>A |
| AA Mutation | p.Arg238His(p.R238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254227 |
| Start | 26911936:26911936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746783997 |
| CDS Mutation | c.683C>T |
| AA Mutation | p.Pro228Leu(p.P228L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254227 |
| Start | 26913543:26913543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.398G>A |
| AA Mutation | p.Gly133Asp(p.G133D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254227 |
| Start | 26913534:26913534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.407C>T |
| AA Mutation | p.Pro136Leu(p.P136L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254227 |
| Start | 26913905:26913905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.36G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254227 |
| Start | 26913491:26913491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139159423 |
| CDS Mutation | c.450A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |