ClinVar Miner

List of variants in gene FKBP10 reported as uncertain significance for Inborn genetic diseases

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_021939.4(FKBP10):c.1667G>A (p.Arg556His) rs138281924 0.00120
NM_021939.4(FKBP10):c.473T>C (p.Val158Ala) rs781874365 0.00009
NM_021939.4(FKBP10):c.1402C>T (p.Arg468Trp) rs542334549 0.00004
NM_021939.4(FKBP10):c.836G>A (p.Cys279Tyr) rs201214666 0.00004
NM_021939.4(FKBP10):c.422A>G (p.Tyr141Cys) rs782600573 0.00001
NM_021939.4(FKBP10):c.1015C>T (p.Arg339Trp) rs377642451
NM_021939.4(FKBP10):c.1034C>T (p.Pro345Leu)
NM_021939.4(FKBP10):c.1087G>C (p.Val363Leu)
NM_021939.4(FKBP10):c.1102G>A (p.Val368Ile)
NM_021939.4(FKBP10):c.112G>T (p.Gly38Trp)
NM_021939.4(FKBP10):c.1146C>G (p.Ile382Met)
NM_021939.4(FKBP10):c.115G>A (p.Gly39Ser) rs142632442
NM_021939.4(FKBP10):c.1577T>A (p.Ile526Asn)
NM_021939.4(FKBP10):c.254G>A (p.Arg85His)
NM_021939.4(FKBP10):c.34C>T (p.Leu12Phe)
NM_021939.4(FKBP10):c.392C>T (p.Ala131Val)
NM_021939.4(FKBP10):c.427G>A (p.Asp143Asn)
NM_021939.4(FKBP10):c.431T>G (p.Val144Gly)
NM_021939.4(FKBP10):c.466G>A (p.Val156Met)
NM_021939.4(FKBP10):c.506G>A (p.Arg169His)
NM_021939.4(FKBP10):c.508A>G (p.Met170Val)
NM_021939.4(FKBP10):c.566C>A (p.Thr189Asn)
NM_021939.4(FKBP10):c.607A>G (p.Thr203Ala)
NM_021939.4(FKBP10):c.608C>A (p.Thr203Asn)
NM_021939.4(FKBP10):c.613G>A (p.Val205Ile)
NM_021939.4(FKBP10):c.674A>G (p.Glu225Gly)
NM_021939.4(FKBP10):c.697C>G (p.Pro233Ala)
NM_021939.4(FKBP10):c.77C>T (p.Ala26Val) rs782067841
NM_021939.4(FKBP10):c.830C>G (p.Pro277Arg)
NM_021939.4(FKBP10):c.841C>T (p.Arg281Cys)
NM_021939.4(FKBP10):c.892A>T (p.Met298Leu)
NM_021939.4(FKBP10):c.932A>C (p.His311Pro)
NM_021939.4(FKBP10):c.941A>G (p.Asn314Ser)
NM_021939.4(FKBP10):c.964A>G (p.Ile322Val)

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