Primary Site >> Stomach Cancer
Gene >> CYP27A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258415 |
| Start | 218812248:218812248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761927223 |
| CDS Mutation | c.473G>A |
| AA Mutation | p.Arg158His(p.R158H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258415 |
| Start | 218809594:218809594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273G>C |
| AA Mutation | p.Lys91Asn(p.K91N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258415 |
| Start | 218812385:218812385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Asp204Asn(p.D204N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258415 |
| Start | 218809677:218809677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.356G>A |
| AA Mutation | p.Arg119Gln(p.R119Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258415 |
| Start | 218809629:218809629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308A>T |
| AA Mutation | p.Gln103Leu(p.Q103L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258415 |
| Start | 218812291:218812291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749708223 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |