Primary Site >> Stomach Cancer
Gene >> G6PD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154546086:154546086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.70G>A |
| AA Mutation | p.Asp24Asn(p.D24N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154534456:154534456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Asp176Asn(p.D176N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154534059:154534059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.746A>G |
| AA Mutation | p.Tyr249Cys(p.Y249C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154532761:154532761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1093C>T |
| AA Mutation | p.Arg365Cys(p.R365C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154535180:154535180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.473G>T |
| AA Mutation | p.Cys158Phe(p.C158F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393564 |
| Start | 154534069:154534069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736C>T |
| AA Mutation | p.Arg246Cys(p.R246C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393564 |
| Start | 154533045:154533045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782587403 |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393564 |
| Start | 154533003:154533003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782064465 |
| CDS Mutation | c.990C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |