Primary Site >> Stomach Cancer
Gene >> ZFP82
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393390:36393390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.950A>C |
| AA Mutation | p.Lys317Thr(p.K317T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36405611:36405611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.198A>C |
| AA Mutation | p.Lys66Asn(p.K66N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393227:36393227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1113T>G |
| AA Mutation | p.Cys371Trp(p.C371W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36392898:36392898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1442A>C |
| AA Mutation | p.Lys481Thr(p.K481T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393287:36393287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1053A>C |
| AA Mutation | p.Gln351His(p.Q351H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36407895:36407895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128T>G |
| AA Mutation | p.Val43Gly(p.V43G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36392758:36392758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1582C>T |
| AA Mutation | p.His528Tyr(p.H528Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393309:36393309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201438784 |
| CDS Mutation | c.1031G>T |
| AA Mutation | p.Gly344Val(p.G344V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393149:36393149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770632054 |
| CDS Mutation | c.1191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393161:36393161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1179T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392161 |
| Start | 36393158:36393158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113215509 |
| CDS Mutation | c.1182C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |