ClinVar Miner

List of variants in gene FN3K reported as uncertain significance for not specified

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_022158.4(FN3K):c.454G>A (p.Gly152Ser) rs144350720 0.00015
NM_022158.4(FN3K):c.823C>G (p.Gln275Glu) rs138224764 0.00012
NM_022158.4(FN3K):c.792C>A (p.His264Gln) rs771241837 0.00011
NM_022158.4(FN3K):c.358A>G (p.Lys120Glu) rs371202212 0.00009
NM_022158.4(FN3K):c.761G>C (p.Gly254Ala) rs779553741 0.00005
NM_022158.4(FN3K):c.854A>C (p.Tyr285Ser) rs770916058 0.00004
NM_022158.4(FN3K):c.905G>C (p.Gly302Ala) rs567326977 0.00004
NM_022158.4(FN3K):c.245G>A (p.Gly82Asp) rs773952542 0.00001
NM_022158.4(FN3K):c.38C>T (p.Thr13Ile) rs1713802046 0.00001
NM_022158.4(FN3K):c.506C>T (p.Ala169Val) rs767158460 0.00001
NM_022158.4(FN3K):c.508C>T (p.Arg170Trp) rs76121523 0.00001
NM_022158.4(FN3K):c.770G>A (p.Arg257Lys) rs377627228 0.00001
NM_022158.4(FN3K):c.794G>A (p.Arg265Gln) rs560630781 0.00001
NM_022158.4(FN3K):c.826C>G (p.Arg276Gly) rs117622449 0.00001
NM_022158.4(FN3K):c.188G>A (p.Arg63Lys)
NM_022158.4(FN3K):c.239C>T (p.Pro80Leu) rs564185306
NM_022158.4(FN3K):c.253G>A (p.Ala85Thr)
NM_022158.4(FN3K):c.31A>T (p.Thr11Ser)
NM_022158.4(FN3K):c.321G>A (p.Met107Ile)
NM_022158.4(FN3K):c.400G>T (p.Gly134Cys) rs1411753546
NM_022158.4(FN3K):c.427T>A (p.Phe143Ile)
NM_022158.4(FN3K):c.430G>A (p.Gly144Ser)
NM_022158.4(FN3K):c.430G>T (p.Gly144Cys)
NM_022158.4(FN3K):c.433T>C (p.Phe145Leu) rs2510320701
NM_022158.4(FN3K):c.440C>T (p.Thr147Met)
NM_022158.4(FN3K):c.49T>G (p.Phe17Val)
NM_022158.4(FN3K):c.524C>T (p.Ala175Val) rs148878409
NM_022158.4(FN3K):c.583C>G (p.Arg195Gly)
NM_022158.4(FN3K):c.602C>T (p.Pro201Leu)
NM_022158.4(FN3K):c.640C>T (p.Leu214Phe)
NM_022158.4(FN3K):c.727G>A (p.Glu243Lys) rs2510325889
NM_022158.4(FN3K):c.7C>G (p.Gln3Glu) rs761200460
NM_022158.4(FN3K):c.807G>C (p.Lys269Asn)
NM_022158.4(FN3K):c.830T>C (p.Leu277Pro)
NM_022158.4(FN3K):c.847T>C (p.Phe283Leu) rs2510326402

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