ClinVar Miner

List of variants in gene NLRP12 reported as uncertain significance for not provided

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Total variants: 77
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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.779C>T (p.Thr260Met) rs150280940 0.00027
NM_144687.4(NLRP12):c.857C>T (p.Pro286Leu) rs201940393 0.00024
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.1854C>G (p.Tyr618Ter) rs142487599 0.00013
NM_144687.4(NLRP12):c.154G>A (p.Gly52Ser) rs369053968 0.00011
NM_144687.4(NLRP12):c.2761G>C (p.Gly921Arg) rs199980950 0.00011
NM_144687.4(NLRP12):c.3000G>C (p.Leu1000Phe) rs201437704 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.986G>A (p.Arg329Gln) rs144287432 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.2183G>A (p.Arg728Gln) rs373285006 0.00006
NM_144687.4(NLRP12):c.2771G>A (p.Arg924Gln) rs570948263 0.00005
NM_144687.4(NLRP12):c.104C>T (p.Ala35Val) rs373357561 0.00004
NM_144687.4(NLRP12):c.2044G>A (p.Ala682Thr) rs778688033 0.00004
NM_144687.4(NLRP12):c.2572C>A (p.Leu858Ile) rs766678083 0.00004
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.2002G>A (p.Ala668Thr) rs1307240172 0.00002
NM_144687.4(NLRP12):c.2120C>T (p.Ala707Val) rs202169378 0.00002
NM_144687.4(NLRP12):c.2363T>G (p.Met788Arg) rs752414417 0.00002
NM_144687.4(NLRP12):c.665G>A (p.Gly222Asp) rs371385297 0.00002
NM_144687.4(NLRP12):c.103G>A (p.Ala35Thr) rs149098000 0.00001
NM_144687.4(NLRP12):c.1546A>G (p.Ser516Gly) rs770763005 0.00001
NM_144687.4(NLRP12):c.1568C>G (p.Ala523Gly) rs1036210460 0.00001
NM_144687.4(NLRP12):c.1572G>A (p.Met524Ile) rs570169359 0.00001
NM_144687.4(NLRP12):c.160C>G (p.Leu54Val) rs764835509 0.00001
NM_144687.4(NLRP12):c.1628G>T (p.Arg543Met) rs1031564464 0.00001
NM_144687.4(NLRP12):c.1752G>C (p.Ser584=) rs769227978 0.00001
NM_144687.4(NLRP12):c.1992C>G (p.His664Gln) rs377549646 0.00001
NM_144687.4(NLRP12):c.2164C>T (p.Arg722Ter) rs750852187 0.00001
NM_144687.4(NLRP12):c.2321G>A (p.Arg774Lys) rs780092868 0.00001
NM_144687.4(NLRP12):c.2750C>T (p.Thr917Ile) rs760120881 0.00001
NM_144687.4(NLRP12):c.2757-1G>T rs143515989 0.00001
NM_144687.4(NLRP12):c.3174C>A (p.Asp1058Glu) rs1690166860 0.00001
NM_144687.4(NLRP12):c.658G>A (p.Gly220Arg) rs781166780 0.00001
NM_144687.4(NLRP12):c.-18G>A rs781775783
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.1196C>G (p.Thr399Ser)
NM_144687.4(NLRP12):c.11C>T (p.Thr4Ile) rs1599879740
NM_144687.4(NLRP12):c.1207G>T (p.Val403Phe) rs765948822
NM_144687.4(NLRP12):c.1346C>G (p.Ala449Gly) rs1016647701
NM_144687.4(NLRP12):c.1538del (p.Ile513fs) rs903100692
NM_144687.4(NLRP12):c.1587C>G (p.Asp529Glu) rs781712648
NM_144687.4(NLRP12):c.1616A>G (p.Gln539Arg) rs1599840470
NM_144687.4(NLRP12):c.1681C>T (p.Arg561Cys) rs747435135
NM_144687.4(NLRP12):c.1991A>G (p.His664Arg)
NM_144687.4(NLRP12):c.2051C>A (p.Ala684Glu) rs753678830
NM_144687.4(NLRP12):c.2072+2dup rs104895565
NM_144687.4(NLRP12):c.2098G>A (p.Ala700Thr)
NM_144687.4(NLRP12):c.2182C>T (p.Arg728Trp) rs764354581
NM_144687.4(NLRP12):c.2216A>C (p.His739Pro) rs778376674
NM_144687.4(NLRP12):c.2368C>T (p.Leu790Phe)
NM_144687.4(NLRP12):c.2480del (p.Pro827fs) rs749913514
NM_144687.4(NLRP12):c.2599C>T (p.Arg867Cys) rs149373778
NM_144687.4(NLRP12):c.2619T>G (p.Cys873Trp)
NM_144687.4(NLRP12):c.2662G>A (p.Glu888Lys)
NM_144687.4(NLRP12):c.3065T>G (p.Leu1022Arg) rs1568654178
NM_144687.4(NLRP12):c.3078_3098+1del rs1064796908
NM_144687.4(NLRP12):c.3088C>G (p.Arg1030Gly) rs201619538
NM_144687.4(NLRP12):c.3161_3162del (p.Lys1054fs) rs1555791815
NM_144687.4(NLRP12):c.337C>G (p.Leu113Val) rs754131900
NM_144687.4(NLRP12):c.358A>C (p.Thr120Pro) rs760912202
NM_144687.4(NLRP12):c.366A>C (p.Arg122Ser)
NM_144687.4(NLRP12):c.455dup (p.Asn152fs) rs759034762
NM_144687.4(NLRP12):c.46dup (p.Tyr16fs) rs1599879570
NM_144687.4(NLRP12):c.616C>T (p.Arg206Cys) rs111754022
NM_144687.4(NLRP12):c.767A>C (p.Asn256Thr) rs867156890
NM_144687.4(NLRP12):c.917C>T (p.Pro306Leu) rs949584865
NM_144687.4(NLRP12):c.994C>A (p.Leu332Met)

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