Primary Site >> Stomach Cancer
Gene >> PDGFRB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150132054:150132054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1168G>A |
| AA Mutation | p.Glu390Lys(p.E390K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150121972:150121972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762698498 |
| CDS Mutation | c.2252A>G |
| AA Mutation | p.Tyr751Cys(p.Y751C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150134878:150134878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Ala168Val(p.A168V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150123141:150123141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375978065 |
| CDS Mutation | c.2084G>A |
| AA Mutation | p.Arg695His(p.R695H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150130642:150130642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1264C>G |
| AA Mutation | p.Leu422Val(p.L422V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150137026:150137026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22C>T |
| AA Mutation | p.Pro8Ser(p.P8S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150133702:150133702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818G>A |
| AA Mutation | p.Arg273His(p.R273H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150117784:150117784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140261309 |
| CDS Mutation | c.2971C>T |
| AA Mutation | p.Arg991Cys(p.R991C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150119521:150119521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754345719 |
| CDS Mutation | c.2744A>G |
| AA Mutation | p.Asn915Ser(p.N915S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150125543:150125543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1709A>C |
| AA Mutation | p.Glu570Ala(p.E570A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150135602:150135602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544478083 |
| CDS Mutation | c.317G>A |
| AA Mutation | p.Arg106His(p.R106H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150121891:150121891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2333A>G |
| AA Mutation | p.Tyr778Cys(p.Y778C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261799 |
| Start | 150117736:150117736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142762235 |
| CDS Mutation | c.3019G>A |
| AA Mutation | p.Val1007Ile(p.V1007I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150126583:150126583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1611C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150118762:150118762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139623802 |
| CDS Mutation | c.2889C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150135823:150135823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.96C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150121899:150121899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2325C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150135637:150135637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150133983:150133983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745467275 |
| CDS Mutation | c.657C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261799 |
| Start | 150120990:150120990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143342011 |
| CDS Mutation | c.2484G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |