Primary Site >> Stomach Cancer
Gene >> ZNF785
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395216 |
| Start | 30582987:30582987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.791G>A |
| AA Mutation | p.Arg264His(p.R264H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395216 |
| Start | 30583140:30583140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.638G>T |
| AA Mutation | p.Arg213Met(p.R213M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395216 |
| Start | 30585202:30585202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254T>C |
| AA Mutation | p.Val85Ala(p.V85A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395216 |
| Start | 30583192:30583192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586G>A |
| AA Mutation | p.Gly196Arg(p.G196R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395216 |
| Start | 30582827:30582827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395216 |
| Start | 30582680:30582680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754271979 |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |