Primary Site >> Stomach Cancer
Gene >> PDGFB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331163 |
| Start | 39235781:39235781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148252800 |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Gly53Arg(p.G53R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331163 |
| Start | 39225793:39225793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.656C>A |
| AA Mutation | p.Pro219His(p.P219H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331163 |
| Start | 39235822:39235822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.116G>A |
| AA Mutation | p.Arg39His(p.R39H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331163 |
| Start | 39233452:39233452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Arg78His(p.R78H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331163 |
| Start | 39225840:39225840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780202003 |
| CDS Mutation | c.609G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331163 |
| Start | 39225762:39225762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540617361 |
| CDS Mutation | c.687G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331163 |
| Start | 39231733:39231733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768635148 |
| CDS Mutation | c.345C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331163 |
| Start | 39231757:39231757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331163 |
| Start | 39231796:39231796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748350476 |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331163 |
| Start | 39225792:39225792(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.657delC |
| AA Mutation | p.Lys220ArgfsTer16(p.K220Rfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |