Primary Site >> Stomach Cancer
Gene >> DMRT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382276 |
| Start | 894128:894128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764065635 |
| CDS Mutation | c.755C>T |
| AA Mutation | p.Pro252Leu(p.P252L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382276 |
| Start | 968111:968111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1094T>C |
| AA Mutation | p.Val365Ala(p.V365A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000382276 |
| Start | 916907:916907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746758951 |
| CDS Mutation | c.967G>A |
| AA Mutation | p.Val323Ile(p.V323I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382276 |
| Start | 894037:894037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.664T>C |
| AA Mutation | p.Tyr222His(p.Y222H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382276 |
| Start | 916875:916875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935A>G |
| AA Mutation | p.Asp312Gly(p.D312G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382276 |
| Start | 847112:847112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200875305 |
| CDS Mutation | c.507G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382276 |
| Start | 841907:841907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762219122 |
| CDS Mutation | c.69G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |