ClinVar Miner

List of variants in gene FKBP14 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_017946.4(FKBP14):c.349+79T>C rs2302626 0.28180
NM_017946.4(FKBP14):c.478-115G>T rs57981260 0.18320
NM_017946.4(FKBP14):c.198-125T>C rs10231351 0.05743
NM_017946.4(FKBP14):c.165C>T (p.Tyr55=) rs17150692 0.01958
NM_017946.4(FKBP14):c.197+23T>C rs17150688 0.01888
NM_017946.4(FKBP14):c.350-275A>G rs117657528 0.00613
NM_017946.4(FKBP14):c.478-290C>T rs77072689 0.00448
NM_017946.4(FKBP14):c.198-324T>C rs77077786 0.00354
NM_017946.4(FKBP14):c.34C>G (p.Leu12Val) rs112905680 0.00310
NM_017946.4(FKBP14):c.349+16T>G rs112323392 0.00272
NM_017946.4(FKBP14):c.478-34A>G rs146517510 0.00260
NM_017946.4(FKBP14):c.495G>A (p.Lys165=) rs142474407 0.00211
NM_017946.4(FKBP14):c.330C>T (p.Gly110=) rs148034796 0.00162
NM_017946.4(FKBP14):c.375G>C (p.Leu125=) rs143268242 0.00150
NM_017946.4(FKBP14):c.123G>A (p.Lys41=) rs149485427 0.00046
NM_017946.4(FKBP14):c.568_570del (p.Lys190del) rs762279651 0.00039
NM_017946.4(FKBP14):c.-22C>T rs77086336 0.00038
NM_017946.4(FKBP14):c.350-8C>T rs368867118 0.00027
NM_017946.4(FKBP14):c.349+15G>A rs201366617 0.00019
NM_017946.4(FKBP14):c.525G>T (p.Val175=) rs747381671 0.00014
NM_017946.4(FKBP14):c.357T>G (p.Ile119Met) rs202182643 0.00010
NM_017946.4(FKBP14):c.350-5G>A rs763069544 0.00007
NM_017946.4(FKBP14):c.*2G>C rs751113052 0.00002
NM_017946.4(FKBP14):c.48_50del (p.Leu17del) rs564626031 0.00002
NM_017946.4(FKBP14):c.206A>G (p.His69Arg) rs564539430 0.00001
NM_017946.4(FKBP14):c.34dup (p.Leu12fs) rs778176957 0.00001
NM_017946.4(FKBP14):c.477+1G>A rs763168158 0.00001
NM_017946.4(FKBP14):c.109A>C (p.Ile37Leu) rs1790174088
NM_017946.4(FKBP14):c.137A>T (p.Asp46Val)
NM_017946.4(FKBP14):c.198-250_198-249insTTAA rs76280627
NM_017946.4(FKBP14):c.247G>A (p.Glu83Lys) rs1264425307
NM_017946.4(FKBP14):c.275T>G (p.Leu92Trp) rs1085307645
NM_017946.4(FKBP14):c.362dup (p.Glu122fs) rs542489955
NM_017946.4(FKBP14):c.410G>C (p.Gly137Ala) rs1554369200
NM_017946.4(FKBP14):c.41T>C (p.Val14Ala)
NM_017946.4(FKBP14):c.493AAG[1] (p.Lys166del) rs542254849
NM_017946.4(FKBP14):c.568A>T (p.Lys190Ter) rs141843195

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