ClinVar Miner

List of variants in gene NLRP12 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.969T>G (p.Leu323=) rs142063194 0.00814
NM_144687.4(NLRP12):c.3046C>T (p.Arg1016Ter) rs35064500 0.00470
NM_144687.4(NLRP12):c.910C>T (p.His304Tyr) rs141245482 0.00392
NM_144687.4(NLRP12):c.960G>A (p.Thr320=) rs77625808 0.00311
NM_144687.4(NLRP12):c.1437G>A (p.Gln479=) rs77667763 0.00294
NM_144687.4(NLRP12):c.2141A>G (p.Asn714Ser) rs150848917 0.00278
NM_144687.4(NLRP12):c.2701G>C (p.Val901Leu) rs104895568 0.00265
NM_144687.4(NLRP12):c.2927+14A>G rs199476247 0.00247
NM_144687.4(NLRP12):c.1299A>G (p.Ala433=) rs73608455 0.00194
NM_144687.4(NLRP12):c.819T>C (p.Pro273=) rs59749540 0.00191
NM_144687.4(NLRP12):c.1352G>A (p.Arg451His) rs76085152 0.00188
NM_144687.4(NLRP12):c.3024C>T (p.Asn1008=) rs140769141 0.00142
NM_144687.3(NLRP12):c.-143C>A rs190223587 0.00121
NM_144687.4(NLRP12):c.2579C>G (p.Thr860Ser) rs150671525 0.00069
NM_144687.3(NLRP12):c.-226A>G rs547032329 0.00058
NM_144687.4(NLRP12):c.559G>A (p.Val187Met) rs147355465 0.00042
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.2673G>A (p.Leu891=) rs201832323 0.00017
NM_144687.4(NLRP12):c.1403G>T (p.Gly468Val) rs559396586 0.00016
NM_144687.4(NLRP12):c.1854C>G (p.Tyr618Ter) rs142487599 0.00013
NM_144687.4(NLRP12):c.2600G>A (p.Arg867His) rs140731275 0.00013
NM_144687.4(NLRP12):c.831G>A (p.Ala277=) rs371391087 0.00013
NM_144687.4(NLRP12):c.2340C>T (p.Asn780=) rs371264069 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.552G>A (p.Ala184=) rs367744369 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.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.752A>G (p.Asn251Ser) rs200679354 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.-2C>G rs142898715 0.00003
NM_144687.4(NLRP12):c.1343G>C (p.Gly448Ala) rs104895566 0.00003
NM_144687.4(NLRP12):c.2052G>A (p.Ala684=) rs755768331 0.00003
NM_144687.4(NLRP12):c.308C>T (p.Pro103Leu) rs141436635 0.00003
NM_144687.4(NLRP12):c.1824G>A (p.Gln608=) rs1308512408 0.00002
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.1035G>A (p.Thr345=) rs770310990 0.00001
NM_144687.4(NLRP12):c.103G>A (p.Ala35Thr) rs149098000 0.00001
NM_144687.4(NLRP12):c.1341G>A (p.Pro447=) rs577056280 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.2757-1G>T rs143515989 0.00001
NM_144687.4(NLRP12):c.2927+10G>A rs759672572 0.00001
NM_144687.4(NLRP12):c.66T>C (p.Ala22=) rs376521503 0.00001
NM_144687.4(NLRP12):c.1196C>G (p.Thr399Ser)
NM_144687.4(NLRP12):c.1197C>T (p.Thr399=)
NM_144687.4(NLRP12):c.1207G>T (p.Val403Phe) rs765948822
NM_144687.4(NLRP12):c.1266dup (p.Leu423fs)
NM_144687.4(NLRP12):c.1346C>G (p.Ala449Gly) rs1016647701
NM_144687.4(NLRP12):c.1681C>T (p.Arg561Cys) rs747435135
NM_144687.4(NLRP12):c.1953G>A (p.Ser651=) rs771048449
NM_144687.4(NLRP12):c.1998T>C (p.Tyr666=) rs1297936600
NM_144687.4(NLRP12):c.2051C>A (p.Ala684Glu) rs753678830
NM_144687.4(NLRP12):c.2072+2dup rs104895565
NM_144687.4(NLRP12):c.2182C>T (p.Arg728Trp) rs764354581
NM_144687.4(NLRP12):c.2186_2187insTT (p.Val730fs) rs1600700389
NM_144687.4(NLRP12):c.2216A>C (p.His739Pro) rs778376674
NM_144687.4(NLRP12):c.2586G>A (p.Trp862Ter) rs1568662444
NM_144687.4(NLRP12):c.2599C>T (p.Arg867Cys) rs149373778
NM_144687.4(NLRP12):c.268C>T (p.Gln90Ter)
NM_144687.4(NLRP12):c.2828_2829dup (p.Arg944fs) rs533054990
NM_144687.4(NLRP12):c.2830C>A (p.Arg944=) rs104895570
NM_144687.4(NLRP12):c.2830C>T (p.Arg944Trp) rs104895570
NM_144687.4(NLRP12):c.2991C>T (p.Asn997=) rs1334288624
NM_144687.4(NLRP12):c.3065T>G (p.Leu1022Arg) rs1568654178
NM_144687.4(NLRP12):c.306C>T (p.Gly102=) rs745452377
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.366A>C (p.Arg122Ser)
NM_144687.4(NLRP12):c.455dup (p.Asn152fs) rs759034762
NM_144687.4(NLRP12):c.627A>G (p.Pro209=) rs2122680445
NM_144687.4(NLRP12):c.917C>T (p.Pro306Leu) rs949584865
NM_144687.4(NLRP12):c.994C>A (p.Leu332Met)

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