ClinVar Miner

List of variants in gene NLRP12 reported as uncertain significance by GeneDx

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.779C>T (p.Thr260Met) rs150280940 0.00027
NM_144687.4(NLRP12):c.1854C>G (p.Tyr618Ter) rs142487599 0.00013
NM_144687.4(NLRP12):c.154G>A (p.Gly52Ser) rs369053968 0.00011
NM_144687.4(NLRP12):c.536C>T (p.Thr179Ile) rs145156267 0.00011
NM_144687.4(NLRP12):c.236G>A (p.Arg79Gln) rs144936138 0.00010
NM_144687.4(NLRP12):c.2575C>T (p.Arg859Trp) rs573629753 0.00009
NM_144687.4(NLRP12):c.1886C>A (p.Ala629Asp) rs146250162 0.00007
NM_144687.4(NLRP12):c.883G>A (p.Gly295Ser) rs768310610 0.00004
NM_144687.4(NLRP12):c.1343G>C (p.Gly448Ala) rs104895566 0.00003
NM_144687.4(NLRP12):c.3151C>T (p.Arg1051Ter) rs199475871 0.00003
NM_144687.4(NLRP12):c.2363T>G (p.Met788Arg) rs752414417 0.00002
NM_144687.4(NLRP12):c.1546A>G (p.Ser516Gly) rs770763005 0.00001
NM_144687.4(NLRP12):c.1572G>A (p.Met524Ile) rs570169359 0.00001
NM_144687.4(NLRP12):c.2750C>T (p.Thr917Ile) rs760120881 0.00001
NM_144687.4(NLRP12):c.658G>A (p.Gly220Arg) rs781166780 0.00001
NM_144687.4(NLRP12):c.1124A>G (p.Tyr375Cys) rs1555796282
NM_144687.4(NLRP12):c.1132T>C (p.Phe378Leu)
NM_144687.4(NLRP12):c.1174A>G (p.Arg392Gly)
NM_144687.4(NLRP12):c.1182C>A (p.Asn394Lys) rs201241894
NM_144687.4(NLRP12):c.1991A>G (p.His664Arg)
NM_144687.4(NLRP12):c.2098G>A (p.Ala700Thr)
NM_144687.4(NLRP12):c.2368C>T (p.Leu790Phe)
NM_144687.4(NLRP12):c.2480del (p.Pro827fs) rs749913514
NM_144687.4(NLRP12):c.2662G>A (p.Glu888Lys)
NM_144687.4(NLRP12):c.3078_3098+1del rs1064796908
NM_144687.4(NLRP12):c.3088C>G (p.Arg1030Gly) rs201619538
NM_144687.4(NLRP12):c.358A>C (p.Thr120Pro) rs760912202
NM_144687.4(NLRP12):c.616C>T (p.Arg206Cys) rs111754022
NM_144687.4(NLRP12):c.767A>C (p.Asn256Thr) rs867156890

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