Primary Site >> Stomach Cancer
Gene >> PPP2R2D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000455566 |
| Start | 131940061:131940061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.229T>C |
| AA Mutation | p.Tyr77His(p.Y77H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000455566 |
| Start | 131955737:131955737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577541215 |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Thr379Met(p.T379M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000455566 |
| Start | 131947672:131947672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.963G>A |
| AA Mutation | p.Met321Ile(p.M321I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000455566 |
| Start | 131955798:131955798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1197A>C |
| AA Mutation | p.Lys399Asn(p.K399N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000455566 |
| Start | 131940692:131940692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781827357 |
| CDS Mutation | c.475C>T |
| AA Mutation | p.Arg159Trp(p.R159W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000455566 |
| Start | 131945383:131945383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567109023 |
| CDS Mutation | c.744C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000455566 |
| Start | 131955738:131955738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181341303 |
| CDS Mutation | c.1137G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |