Primary Site >> Stomach Cancer
Gene >> FOXK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4740975:4740975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698A>G |
| AA Mutation | p.Asp233Gly(p.D233G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4761258:4761258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1891C>T |
| AA Mutation | p.Pro631Ser(p.P631S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4759397:4759397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766885716 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Ala500Thr(p.A500T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4761096:4761096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1729A>G |
| AA Mutation | p.Thr577Ala(p.T577A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4761088:4761088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1721C>T |
| AA Mutation | p.Ala574Val(p.A574V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328914 |
| Start | 4682765:4682765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.457T>G |
| AA Mutation | p.Phe153Val(p.F153V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328914 |
| Start | 4761107:4761107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780896615 |
| CDS Mutation | c.1740G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328914 |
| Start | 4754537:4754537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.825C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328914 |
| Start | 4761089:4761089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200211699 |
| CDS Mutation | c.1722G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328914 |
| Start | 4754489:4754489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767558881 |
| CDS Mutation | c.777C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |