Primary Site >> Stomach Cancer
Gene >> CD82
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227155 |
| Start | 44605400:44605400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574662941 |
| CDS Mutation | c.307G>A |
| AA Mutation | p.Gly103Arg(p.G103R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227155 |
| Start | 44618697:44618697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755430626 |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Val234Met(p.V234M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227155 |
| Start | 44618343:44618343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.620A>G |
| AA Mutation | p.Glu207Gly(p.E207G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227155 |
| Start | 44615320:44615320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.385A>T |
| AA Mutation | p.Asn129Tyr(p.N129Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227155 |
| Start | 44605165:44605165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.244C>T |
| AA Mutation | p.Arg82Cys(p.R82C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227155 |
| Start | 44618173:44618173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150371864 |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |