Primary Site >> Stomach Cancer
Gene >> HSD3B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514302:119514302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142647336 |
| CDS Mutation | c.779C>T |
| AA Mutation | p.Thr260Met(p.T260M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514473:119514473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374232920 |
| CDS Mutation | c.950G>A |
| AA Mutation | p.Arg317His(p.R317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514191:119514191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668C>T |
| AA Mutation | p.Pro223Leu(p.P223L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369413 |
| Start | 119507481:119507481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370361626 |
| CDS Mutation | c.5C>T |
| AA Mutation | p.Thr2Met(p.T2M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514054:119514054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190598307 |
| CDS Mutation | c.531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514051:119514051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749065451 |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369413 |
| Start | 119511582:119511582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587677852 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369413 |
| Start | 119514046:119514046(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.527delA |
| AA Mutation | p.Asn176ThrfsTer27(p.N176Tfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369413 |
| Start | 119513966:119513966(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.446delA |
| AA Mutation | p.Asn149ThrfsTer26(p.N149Tfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |