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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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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.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.2761G>C (p.Gly921Arg)	rs199980950	0.00011
NM_144687.4(NLRP12):c.3000G>C (p.Leu1000Phe)	rs201437704	0.00011
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.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.1343G>C (p.Gly448Ala)	rs104895566	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.103G>A (p.Ala35Thr)	rs149098000	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.1196C>G (p.Thr399Ser)
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.1681C>T (p.Arg561Cys)	rs747435135
NM_144687.4(NLRP12):c.2051C>A (p.Ala684Glu)	rs753678830
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.2599C>T (p.Arg867Cys)	rs149373778
NM_144687.4(NLRP12):c.3065T>G (p.Leu1022Arg)	rs1568654178
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.917C>T (p.Pro306Leu)	rs949584865
NM_144687.4(NLRP12):c.994C>A (p.Leu332Met)

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