ClinVar Miner

List of variants in gene FECH reported as uncertain significance for not provided

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_000140.5(FECH):c.185C>G (p.Pro62Arg) rs150830931 0.00124
NM_000140.5(FECH):c.801G>A (p.Met267Ile) rs118204037 0.00108
NM_000140.5(FECH):c.959A>G (p.Lys320Arg) rs371224528 0.00007
NM_000140.5(FECH):c.1147G>A (p.Asp383Asn) rs769047929 0.00004
NM_000140.5(FECH):c.1213C>T (p.Leu405Phe) rs371363582 0.00001
NM_000140.5(FECH):c.346A>C (p.Thr116Pro) rs1422688348 0.00001
NM_000140.5(FECH):c.599-3C>T rs765069812 0.00001
NM_000140.5(FECH):c.104G>A (p.Arg35Lys)
NM_000140.5(FECH):c.112T>G (p.Ser38Ala) rs2051255745
NM_000140.5(FECH):c.1136A>G (p.Lys379Arg)
NM_000140.5(FECH):c.1253T>G (p.Phe418Cys) rs767086949
NM_000140.5(FECH):c.155A>T (p.His52Leu) rs1413953115
NM_000140.5(FECH):c.163G>T (p.Gly55Cys) rs3848519
NM_000140.5(FECH):c.232G>A (p.Gly78Ser)
NM_000140.5(FECH):c.307A>C (p.Ile103Leu) rs2122329449
NM_000140.5(FECH):c.314+6A>G
NM_000140.5(FECH):c.451T>C (p.Ser151Pro)
NM_000140.5(FECH):c.452C>T (p.Ser151Phe) rs765875996
NM_000140.5(FECH):c.479A>G (p.Tyr160Cys)
NM_000140.5(FECH):c.490C>T (p.Arg164Trp)
NM_000140.5(FECH):c.581A>G (p.Tyr194Cys)
NM_000140.5(FECH):c.586T>C (p.Cys196Arg)
NM_000140.5(FECH):c.589T>A (p.Ser197Thr)
NM_000140.5(FECH):c.590C>T (p.Ser197Phe)
NM_000140.5(FECH):c.598+3A>G
NM_000140.5(FECH):c.613G>A (p.Ala205Thr)
NM_000140.5(FECH):c.643C>T (p.Arg215Trp)
NM_000140.5(FECH):c.656T>G (p.Met219Arg)
NM_000140.5(FECH):c.665G>A (p.Ser222Asn) rs2122284610
NM_000140.5(FECH):c.671T>C (p.Ile224Thr)
NM_000140.5(FECH):c.689A>C (p.His230Pro)
NM_000140.5(FECH):c.793C>G (p.Leu265Val)
NM_000140.5(FECH):c.803C>T (p.Ser268Phe)
NM_000140.5(FECH):c.804+5G>A
NM_000140.5(FECH):c.815G>A (p.Arg272Lys)
NM_000140.5(FECH):c.836A>T (p.Glu279Val) rs2122250951
NM_000140.5(FECH):c.885C>A (p.Asn295Lys)
NM_000140.5(FECH):c.947A>G (p.Asp316Gly)

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