Primary Site >> Stomach Cancer
Gene >> GJA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447051:121447051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.204G>C |
| AA Mutation | p.Lys68Asn(p.K68N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121446957:121446957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.110T>C |
| AA Mutation | p.Leu37Pro(p.L37P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447349:121447349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2228961 |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Ala168Thr(p.A168T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447493:121447493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646G>C |
| AA Mutation | p.Val216Leu(p.V216L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447874:121447874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1027A>C |
| AA Mutation | p.Asn343His(p.N343H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447377:121447377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530A>G |
| AA Mutation | p.Tyr177Cys(p.Y177C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447629:121447629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.782G>T |
| AA Mutation | p.Gly261Val(p.G261V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447452:121447452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750294638 |
| CDS Mutation | c.605G>A |
| AA Mutation | p.Arg202His(p.R202H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447562:121447562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Trp(p.R239W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447275:121447275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.428G>A |
| AA Mutation | p.Gly143Asp(p.G143D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447741:121447741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447792:121447792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447552:121447552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746726971 |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282561 |
| Start | 121447621:121447621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758166001 |
| CDS Mutation | c.774A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |