Primary Site >> Stomach Cancer
Gene >> CSF2RA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1290423:1290423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758879393 |
| CDS Mutation | c.560C>T |
| AA Mutation | p.Thr187Met(p.T187M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1294370:1294370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371464087 |
| CDS Mutation | c.689C>T |
| AA Mutation | p.Thr230Met(p.T230M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1309445:1309445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749182596 |
| CDS Mutation | c.1169G>A |
| AA Mutation | p.Arg390His(p.R390H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1294361:1294361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761247845 |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227His(p.R227H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1285810:1285810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775556939 |
| CDS Mutation | c.109A>G |
| AA Mutation | p.Asn37Asp(p.N37D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1300525:1300525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845A>G |
| AA Mutation | p.Asn282Ser(p.N282S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1282741:1282741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.38T>C |
| AA Mutation | p.Leu13Ser(p.L13S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1288773:1288773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148928173 |
| CDS Mutation | c.358G>A |
| AA Mutation | p.Ala120Thr(p.A120T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1290468:1290468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605G>T |
| AA Mutation | p.Gly202Val(p.G202V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381524 |
| Start | 1303992:1303992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Gly339Asp(p.G339D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381524 |
| Start | 1309446:1309446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770943329 |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381524 |
| Start | 1290415:1290415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144461474 |
| CDS Mutation | c.552A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381524 |
| Start | 1294422:1294422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761160075 |
| CDS Mutation | c.741G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |