List of variants in gene NLRP12 reported as likely benign by Illumina Laboratory Services, Illumina

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: 23

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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_144687.3(NLRP12):c.*362G>T	rs562576939	0.00280
NM_144687.4(NLRP12):c.2141A>G (p.Asn714Ser)	rs150848917	0.00278
NM_001277126.1(NLRP12):c.*471A>G	rs544178725	0.00175
NM_144687.4(NLRP12):c.2757-8C>G	rs370391218	0.00025
NM_144687.4(NLRP12):c.629C>T (p.Pro210Leu)	rs377594629	0.00021
NM_144687.4(NLRP12):c.2212A>C (p.Arg738=)	rs199966186	0.00016
NM_144687.4(NLRP12):c.2748G>A (p.Gln916=)	rs368633277	0.00013
NM_144687.4(NLRP12):c.2761G>C (p.Gly921Arg)	rs199980950	0.00011
NM_144687.4(NLRP12):c.986G>A (p.Arg329Gln)	rs144287432	0.00010
NM_144687.4(NLRP12):c.1349C>T (p.Pro450Leu)	rs143640165	0.00009
NM_144687.4(NLRP12):c.2831G>A (p.Arg944Gln)	rs200742741	0.00009
NM_144687.4(NLRP12):c.2120C>T (p.Ala707Val)	rs202169378	0.00002
NM_144687.4(NLRP12):c.2499C>A (p.Asp833Glu)	rs139956424	0.00002
NM_144687.4(NLRP12):c.2792A>G (p.Glu931Gly)	rs566677129	0.00002
NM_144687.4(NLRP12):c.538G>A (p.Gly180Ser)	rs563974183	0.00002
NM_144687.4(NLRP12):c.1461C>T (p.Asp487=)	rs555808644
NM_144687.4(NLRP12):c.2182C>T (p.Arg728Trp)	rs764354581
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.2927+4_2927+5dup	rs763190690
NM_144687.4(NLRP12):c.616C>T (p.Arg206Cys)	rs111754022

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