Primary Site >> Stomach Cancer
Gene >> HSP90AA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102085425:102085425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.536C>A |
| AA Mutation | p.Pro179His(p.P179H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102084698:102084698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.964G>A |
| AA Mutation | p.Asp322Asn(p.D322N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102086031:102086031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.256G>T |
| AA Mutation | p.Asp86Tyr(p.D86Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102084814:102084814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848A>C |
| AA Mutation | p.Lys283Thr(p.K283T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102083972:102083972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1159G>T |
| AA Mutation | p.Gly387Trp(p.G387W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102086021:102086021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.266T>C |
| AA Mutation | p.Leu89Pro(p.L89P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102084425:102084425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Cys374Tyr(p.C374Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216281 |
| Start | 102085938:102085938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.349G>T |
| AA Mutation | p.Ala117Ser(p.A117S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334701 |
| Start | 102101980:102101980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768847708 |
| CDS Mutation | c.261C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000216281 |
| Start | 102082232:102082234(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1966_1968delGAC |
| AA Mutation | p.Asp656del(p.D656del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |