Primary Site >> Stomach Cancer
Gene >> PPP1R3D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939516:59939516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.416C>T |
| AA Mutation | p.Ser139Leu(p.S139L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939093:59939093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839G>A |
| AA Mutation | p.Arg280His(p.R280H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939337:59939337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.595G>A |
| AA Mutation | p.Ala199Thr(p.A199T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939270:59939270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Ala221Val(p.A221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939260:59939260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370996 |
| Start | 59939140:59939140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146169621 |
| CDS Mutation | c.792C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |