Primary Site >> Stomach Cancer
Gene >> PPP1R7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234038 |
| Start | 241182683:241182683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Asp315Asn(p.D315N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234038 |
| Start | 241166380:241166380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.758A>G |
| AA Mutation | p.Asn253Ser(p.N253S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234038 |
| Start | 241166416:241166416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794A>C |
| AA Mutation | p.Glu265Ala(p.E265A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234038 |
| Start | 241166409:241166409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787G>T |
| AA Mutation | p.Gly263Cys(p.G263C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234038 |
| Start | 241150517:241150517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.22G>A |
| AA Mutation | p.Gly8Arg(p.G8R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234038 |
| Start | 241153584:241153584(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.166delG |
| AA Mutation | p.Glu56ArgfsTer28(p.E56Rfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000234038 |
| Start | 241163283:241163283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111491483 |
| CDS Mutation | c.598-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |