FRK
fyn related Src family tyrosine kinase
Summary
The protein encoded by this gene belongs to the TYR family of protein kinases. This tyrosine kinase is a nuclear protein and may function during G1 and S phase of the cell cycle and suppress growth. [provided by RefSeq, Jul 2008]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1246276760 | 6:116,263,609 | A/G | — | uncertain significance |
| rs777464965 | 6:116,264,209 | A/G | — | uncertain significance |
| rs141208044 | 6:116,264,236 | G/C | — | uncertain significance |
| rs2533576474 | 6:116,264,266 | T/C | — | uncertain significance |
| rs377733382 | 6:116,264,272 | C/T | — | uncertain significance |
| rs374511452 | 6:116,264,282 | C/T | — | uncertain significance |
| rs201586564 | 6:116,265,493 | G/T | — | uncertain significance |
| rs765942689 | 6:116,265,577 | A/G | — | uncertain significance |
| rs184128865 | 6:116,287,196 | T/C | intron variant | — |
| rs145089105 | 6:116,288,825 | C/T | — | uncertain significance |
| rs917697615 | 6:116,289,840 | G/T | — | uncertain significance |
| rs764595423 | 6:116,289,885 | C/T | — | uncertain significance |
| rs143351471 | 6:116,289,888 | C/T | — | uncertain significance |
| rs1293222319 | 6:116,289,891 | C/A | — | uncertain significance |
| rs1933737 | 6:116,310,287 | T/C | intron variant | — |
| rs36061333 | 6:116,311,763 | C/G | intron variant | — |
| rs9488822 | 6:116,312,893 | A/T | intron variant | — |
| rs3822855 | 6:116,316,882 | G/T | intron variant | — |
| rs3822854 | 6:116,316,896 | A/T | — | — |
| rs6934962 | 6:116,322,349 | C/T | intron variant | — |
| rs1338667 | 6:116,323,910 | T/A | intron variant | — |
| rs151309696 | 6:116,325,050 | G/C | — | uncertain significance |
| rs1016330218 | 6:116,325,079 | T/C | — | uncertain significance |
| rs762257926 | 6:116,325,090 | G/A | — | uncertain significance |
| rs770246096 | 6:116,325,094 | C/T | — | uncertain significance |
| rs2533788318 | 6:116,325,097 | T/A | — | uncertain significance |
| rs1538385 | 6:116,327,493 | A/G | intron variant | — |
| rs2351285 | 6:116,327,861 | C/T | intron variant | — |
| rs4354188 | 6:116,327,936 | T/C | intron variant | — |
| rs11153591 | 6:116,328,533 | A/T | intron variant | — |
| rs1890426 | 6:116,338,065 | T/C | regulatory region variant | — |
| rs952373 | 6:116,350,788 | G/T | — | — |
| rs6909746 | 6:116,352,750 | C/T | intron variant | — |
| rs7773423 | 6:116,363,149 | A/C | — | — |
| rs2533981444 | 6:116,381,260 | A/G | — | uncertain significance |
| rs200539604 | 6:116,381,349 | C/A | — | uncertain significance |
| rs377628003 | 6:116,381,413 | G/A | — | uncertain significance |
| rs1999930 | 6:116,387,134 | C/G | — | — |
| rs1933736 | 6:116,387,255 | T/C | intergenic variant | — |
| rs72951954 | 6:116,393,727 | C/A | — | — |
| rs13194714 | 6:116,394,819 | T/A | intergenic variant | — |
| rs6932852 | 6:116,399,372 | C/T | intergenic variant | — |
| rs9374591 | 6:116,410,614 | T/C | intergenic variant | — |
| rs720446 | 6:116,419,124 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.