Primary Site >> Stomach Cancer
Gene >> PPM1D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663256:60663256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1522A>G |
| AA Mutation | p.Met508Val(p.M508V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663389:60663389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760201595 |
| CDS Mutation | c.1655G>A |
| AA Mutation | p.Arg552Gln(p.R552Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305921 |
| Start | 60623700:60623700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652A>G |
| AA Mutation | p.Lys218Glu(p.K218E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305921 |
| Start | 60656690:60656690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109C>T |
| AA Mutation | p.Ala370Val(p.A370V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663053:60663053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319T>C |
| AA Mutation | p.Val440Ala(p.V440A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663528:60663528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1794C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663263:60663263(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766595966 |
| CDS Mutation | c.1535delA |
| AA Mutation | p.Asn512IlefsTer2(p.N512Ifs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305921 |
| Start | 60663078:60663078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758630849 |
| CDS Mutation | c.1349delT |
| AA Mutation | p.Leu450Ter(p.L450*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000305921 |
| Start | 60663106:60663106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773389405 |
| CDS Mutation | c.1372C>T |
| AA Mutation | p.Arg458Ter(p.R458*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |