ClinVar Miner

List of variants in gene HGF reported as uncertain significance by GeneDx

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_000601.6(HGF):c.682T>G (p.Ser228Ala) rs139457161 0.00017
NM_000601.6(HGF):c.1934A>G (p.His645Arg) rs202215700 0.00009
NM_000601.6(HGF):c.983G>A (p.Arg328His) rs374484762 0.00009
NM_000601.6(HGF):c.659G>A (p.Arg220Gln) rs372600489 0.00005
NM_000601.6(HGF):c.2105G>A (p.Arg702His) rs763933267 0.00002
NM_000601.6(HGF):c.1735C>G (p.Leu579Val) rs1789424748 0.00001
NM_000601.6(HGF):c.2084G>A (p.Arg695His) rs543827901 0.00001
NM_000601.6(HGF):c.400C>T (p.Arg134Cys) rs1032300573 0.00001
NM_000601.6(HGF):c.6G>T (p.Trp2Cys) rs745851853 0.00001
NM_000601.6(HGF):c.725G>A (p.Arg242Gln) rs200559590 0.00001
NM_000601.6(HGF):c.104GAA[1] (p.Arg36del) rs771230803
NM_000601.6(HGF):c.1066A>C (p.Asn356His)
NM_000601.6(HGF):c.1072G>A (p.Asp358Asn)
NM_000601.6(HGF):c.1154T>C (p.Met385Thr) rs2115903547
NM_000601.6(HGF):c.1518A>G (p.Gly506=)
NM_000601.6(HGF):c.1553T>C (p.Ile518Thr)
NM_000601.6(HGF):c.1765G>C (p.Val589Leu)
NM_000601.6(HGF):c.1981G>A (p.Ala661Thr) rs769580628
NM_000601.6(HGF):c.2141A>G (p.Lys714Arg) rs2535209715
NM_000601.6(HGF):c.238C>T (p.Leu80Phe)
NM_000601.6(HGF):c.401G>A (p.Arg134His)
NM_000601.6(HGF):c.502C>T (p.Arg168Trp)
NM_000601.6(HGF):c.503G>A (p.Arg168Gln)
NM_000601.6(HGF):c.557G>A (p.Gly186Glu)
NM_000601.6(HGF):c.754G>A (p.Asp252Asn) rs752123971
NM_000601.6(HGF):c.754G>C (p.Asp252His) rs752123971
NM_000601.6(HGF):c.76A>G (p.Ile26Val)
NM_000601.6(HGF):c.792T>A (p.Asp264Glu)
NM_000601.6(HGF):c.802A>G (p.Arg268Gly)
NM_000601.6(HGF):c.832A>G (p.Thr278Ala)
NM_000601.6(HGF):c.854T>C (p.Ile285Thr)
NM_000601.6(HGF):c.860C>T (p.Thr287Ile)
NM_000601.6(HGF):c.992C>T (p.Ser331Phe)

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