Primary Site >> Stomach Cancer
Gene >> FOXP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 71041458:71041458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.739A>G |
| AA Mutation | p.Asn247Asp(p.N247D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70976948:70976948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1523C>T |
| AA Mutation | p.Thr508Met(p.T508M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70965949:70965949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1830G>T |
| AA Mutation | p.Met610Ile(p.M610I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70976951:70976951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1520C>G |
| AA Mutation | p.Ala507Gly(p.A507G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70977866:70977866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1310G>T |
| AA Mutation | p.Arg437Met(p.R437M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 71198252:71198252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540360773 |
| CDS Mutation | c.130G>A |
| AA Mutation | p.Val44Met(p.V44M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 71041335:71041335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.862A>G |
| AA Mutation | p.Arg288Gly(p.R288G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70978010:70978010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1166T>C |
| AA Mutation | p.Val389Ala(p.V389A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70965930:70965930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1849G>A |
| AA Mutation | p.Glu617Lys(p.E617K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70972598:70972598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1609G>A |
| AA Mutation | p.Asp537Asn(p.D537N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 71047087:71047087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.519G>T |
| AA Mutation | p.Gln173His(p.Q173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318789 |
| Start | 70977942:70977942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200629338 |
| CDS Mutation | c.1234G>A |
| AA Mutation | p.Ala412Thr(p.A412T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318789 |
| Start | 70959280:70959280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772162873 |
| CDS Mutation | c.2001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318789 |
| Start | 71198295:71198295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550457312 |
| CDS Mutation | c.87C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318789 |
| Start | 70965958:70965958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768285337 |
| CDS Mutation | c.1821C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318789 |
| Start | 71198259:71198259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201155996 |
| CDS Mutation | c.123G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |