Primary Site >> Stomach Cancer
Gene >> PSMD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264639 |
| Start | 39990144:39990144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928A>G |
| AA Mutation | p.Thr310Ala(p.T310A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264639 |
| Start | 39986660:39986660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497A>G |
| AA Mutation | p.Tyr166Cys(p.Y166C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264639 |
| Start | 39997517:39997517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Arg514Gln(p.R514Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264639 |
| Start | 39997560:39997560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1584T>A |
| AA Mutation | p.Asp528Glu(p.D528E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264639 |
| Start | 39986628:39986628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576377128 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264639 |
| Start | 39995270:39995270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764061023 |
| CDS Mutation | c.1191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |