Primary Site >> Stomach Cancer
Gene >> PPP1R3B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141141:9141141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.511A>C |
| AA Mutation | p.Ser171Arg(p.S171R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141468:9141468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768094652 |
| CDS Mutation | c.184C>T |
| AA Mutation | p.Arg62Trp(p.R62W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141462:9141462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.190T>C |
| AA Mutation | p.Ser64Pro(p.S64P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141600:9141600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376926182 |
| CDS Mutation | c.52C>T |
| AA Mutation | p.Arg18Cys(p.R18C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141006:9141006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646T>C |
| AA Mutation | p.Cys216Arg(p.C216R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141297:9141297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771689160 |
| CDS Mutation | c.355G>A |
| AA Mutation | p.Ala119Thr(p.A119T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310455 |
| Start | 9141157:9141157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138887555 |
| CDS Mutation | c.495G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |