Primary Site >> Stomach Cancer
Gene >> GJB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241124 |
| Start | 20223141:20223141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754990415 |
| CDS Mutation | c.340G>T |
| AA Mutation | p.Asp114Tyr(p.D114Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241124 |
| Start | 20223275:20223275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206T>C |
| AA Mutation | p.Phe69Ser(p.F69S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241124 |
| Start | 20223206:20223206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275C>T |
| AA Mutation | p.Ala92Val(p.A92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241124 |
| Start | 20223077:20223077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404C>T |
| AA Mutation | p.Thr135Met(p.T135M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241124 |
| Start | 20222983:20222983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241124 |
| Start | 20223466:20223466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150075979 |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |