Primary Site >> Stomach Cancer
Gene >> GJA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794913:34794913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700C>T |
| AA Mutation | p.Arg234Cys(p.R234C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794911:34794911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758492393 |
| CDS Mutation | c.698G>A |
| AA Mutation | p.Cys233Tyr(p.C233Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794573:34794573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.360C>A |
| AA Mutation | p.Asp120Glu(p.D120E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794553:34794553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758289830 |
| CDS Mutation | c.340C>T |
| AA Mutation | p.Arg114Trp(p.R114W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34795144:34795144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.931C>T |
| AA Mutation | p.Pro311Ser(p.P311S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34795177:34795177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750895718 |
| CDS Mutation | c.964C>T |
| AA Mutation | p.Arg322Cys(p.R322C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794328:34794328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.115C>A |
| AA Mutation | p.Leu39Met(p.L39M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342280 |
| Start | 34794267:34794267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143380983 |
| CDS Mutation | c.54G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |