Primary Site >> Stomach Cancer
Gene >> PDGFRA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54263720:54263720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421G>A |
| AA Mutation | p.Glu141Lys(p.E141K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54263700:54263700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373126818 |
| CDS Mutation | c.401C>T |
| AA Mutation | p.Thr134Met(p.T134M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54280387:54280387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2228T>C |
| AA Mutation | p.Val743Ala(p.V743A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54295252:54295252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3250G>A |
| AA Mutation | p.Val1084Met(p.V1084M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54272501:54272501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345A>G |
| AA Mutation | p.Ile449Val(p.I449V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54273688:54273688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1516C>A |
| AA Mutation | p.Leu506Ile(p.L506I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54277435:54277435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1834G>A |
| AA Mutation | p.Ala612Thr(p.A612T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54267558:54267558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.938G>T |
| AA Mutation | p.Gly313Val(p.G313V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54280345:54280345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2186G>T |
| AA Mutation | p.Gly729Val(p.G729V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54263759:54263759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.460G>T |
| AA Mutation | p.Asp154Tyr(p.D154Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54267374:54267374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845T>C |
| AA Mutation | p.Val282Ala(p.V282A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257290 |
| Start | 54272445:54272445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202072966 |
| CDS Mutation | c.1289G>A |
| AA Mutation | p.Gly430Glu(p.G430E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54273699:54273699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1527T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54261321:54261321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140725151 |
| CDS Mutation | c.276G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54274550:54274550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142562038 |
| CDS Mutation | c.1578G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54264980:54264980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.690G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54288881:54288881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2757C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54267637:54267637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1017G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54290417:54290417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138801854 |
| CDS Mutation | c.2985C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54280451:54280451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2292T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257290 |
| Start | 54273621:54273621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759936321 |
| CDS Mutation | c.1449C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257290 |
| Start | 54288805:54288805(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2684delC |
| AA Mutation | p.Pro895LeufsTer5(p.P895Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257290 |
| Start | 54261339:54261339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.294C>A |
| AA Mutation | p.Tyr98Ter(p.Y98*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |