Primary Site >> Stomach Cancer
Gene >> FOXC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320354 |
| Start | 86568651:86568651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1316C>G |
| AA Mutation | p.Thr439Arg(p.T439R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567603:86567603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Glu90Lys(p.E90K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567405:86567405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.70T>C |
| AA Mutation | p.Tyr24His(p.Y24H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567997:86567997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Ala221Val(p.A221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567617:86567617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759417459 |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320354 |
| Start | 86568682:86568682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778599000 |
| CDS Mutation | c.1347C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567554:86567554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754671977 |
| CDS Mutation | c.219G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320354 |
| Start | 86567452:86567452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.117C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320354 |
| Start | 86568361:86568361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755617186 |
| CDS Mutation | c.1026C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000320354 |
| Start | 86567633:86567633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298C>T |
| AA Mutation | p.Gln100Ter(p.Q100*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |