ClinVar Miner

List of variants in gene NLRP12 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.3046C>T (p.Arg1016Ter) rs35064500 0.00470
NM_144687.4(NLRP12):c.850C>T (p.Arg284Ter) rs104895564 0.00044
NM_144687.4(NLRP12):c.1022C>T (p.Thr341Ile) rs200996095 0.00019
NM_144687.4(NLRP12):c.1054C>T (p.Arg352Cys) rs199881207 0.00019
NM_144687.4(NLRP12):c.1756C>T (p.His586Tyr) rs772704000 0.00006
NM_144687.4(NLRP12):c.2183G>A (p.Arg728Gln) rs373285006 0.00006
NM_144687.4(NLRP12):c.2966A>C (p.Asn989Thr) rs151187420 0.00006
NM_144687.4(NLRP12):c.1951T>C (p.Ser651Pro) rs370478544 0.00005
NM_144687.4(NLRP12):c.104C>T (p.Ala35Val) rs373357561 0.00004
NM_144687.4(NLRP12):c.1102G>A (p.Ala368Thr) rs541068679 0.00004
NM_144687.4(NLRP12):c.1855G>A (p.Glu619Lys) rs139082917 0.00004
NM_144687.4(NLRP12):c.448T>A (p.Cys150Ser) rs746324074 0.00001
NM_144687.4(NLRP12):c.653C>T (p.Ala218Val) rs749659859 0.00001
NM_144687.4(NLRP12):c.964C>G (p.Leu322Val) rs745451806 0.00001
NM_144687.4(NLRP12):c.1894C>T (p.His632Tyr) rs1600706886
NM_144687.4(NLRP12):c.1952C>A (p.Ser651Ter) rs781361326
NM_144687.4(NLRP12):c.2602C>T (p.Leu868Phe) rs1600683649
NM_144687.4(NLRP12):c.2754G>A (p.Leu918=) rs61741347
NM_144687.4(NLRP12):c.3088C>G (p.Arg1030Gly) rs201619538
NM_144687.4(NLRP12):c.617G>A (p.Arg206His) rs139461508

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