Primary Site >> Stomach Cancer
Gene >> DHRS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250383 |
| Start | 23638989:23638989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2295908 |
| CDS Mutation | c.125C>T |
| AA Mutation | p.Thr42Met(p.T42M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250383 |
| Start | 23643192:23643192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754590049 |
| CDS Mutation | c.461G>A |
| AA Mutation | p.Ser154Asn(p.S154N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250383 |
| Start | 23644521:23644521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.653T>C |
| AA Mutation | p.Ile218Thr(p.I218T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250383 |
| Start | 23639317:23639317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775450619 |
| CDS Mutation | c.279C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250383 |
| Start | 23644489:23644489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778936300 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250383 |
| Start | 23644477:23644477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.609G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |