ClinVar Miner

List of variants in gene GPC3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_004484.4(GPC3):c.359G>A (p.Arg120His) rs148021273 0.00052
NM_004484.4(GPC3):c.660C>T (p.Ser220=) rs138450923 0.00050
NM_004484.4(GPC3):c.1254C>T (p.Asn418=) rs150766741 0.00032
NM_004484.4(GPC3):c.1713G>A (p.Ser571=) rs149209315 0.00024
NM_004484.4(GPC3):c.176-40G>C rs371396859 0.00020
NM_004484.4(GPC3):c.172C>T (p.Pro58Ser) rs147231796 0.00014
NM_004484.4(GPC3):c.1232G>T (p.Ser411Ile) rs139206747 0.00010
NM_004484.4(GPC3):c.358C>T (p.Arg120Cys) rs587778392 0.00006
NM_004484.4(GPC3):c.168C>G (p.Pro56=) rs188592483 0.00005
NM_004484.4(GPC3):c.1632G>A (p.Pro544=) rs766482434 0.00004
NM_004484.4(GPC3):c.414T>C (p.Thr138=) rs1048793393 0.00004
NM_004484.4(GPC3):c.972T>C (p.Phe324=) rs183678432 0.00004
NM_004484.4(GPC3):c.1068A>G (p.Gln356=) rs372212269 0.00002
NM_004484.4(GPC3):c.1162A>G (p.Arg388Gly) rs199812705 0.00001
NM_004484.4(GPC3):c.1641C>T (p.Asn547=) rs772217919 0.00001
NM_004484.4(GPC3):c.1033-4250T>C
NM_004484.4(GPC3):c.1166+8G>T rs2124437393
NM_004484.4(GPC3):c.1284C>T (p.Leu428=) rs2124430679
NM_004484.4(GPC3):c.1566C>T (p.Phe522=)
NM_004484.4(GPC3):c.1574-7_1574-4del rs751413609
NM_004484.4(GPC3):c.1665C>T (p.Leu555=) rs1248944051

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