List of variants in gene NLRP12 reported as likely benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.956C>G (p.Pro319Arg)	rs35401786	0.00803
NM_144687.4(NLRP12):c.424G>A (p.Asp142Asn)	rs34330210	0.00799
NM_144687.4(NLRP12):c.2754G>C (p.Leu918=)	rs61741347	0.00692
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.1299A>G (p.Ala433=)	rs73608455	0.00194
NM_144687.4(NLRP12):c.1352G>A (p.Arg451His)	rs76085152	0.00188
NM_144687.4(NLRP12):c.2227A>C (p.Lys743Gln)	rs74373537	0.00180
NM_144687.4(NLRP12):c.3024C>T (p.Asn1008=)	rs140769141	0.00142
NM_144687.4(NLRP12):c.3004G>A (p.Asp1002Asn)	rs144746100	0.00131
NM_144687.4(NLRP12):c.1731G>A (p.Lys577=)	rs73608454	0.00126
NM_144687.4(NLRP12):c.2579C>G (p.Thr860Ser)	rs150671525	0.00069
NM_144687.4(NLRP12):c.291T>C (p.Asp97=)	rs201046901	0.00027
NM_144687.4(NLRP12):c.1054C>T (p.Arg352Cys)	rs199881207	0.00019
NM_144687.4(NLRP12):c.1790G>A (p.Ser597Asn)	rs748314396	0.00008
NM_144687.4(NLRP12):c.1599C>T (p.Gly533=)	rs758678359	0.00006
NM_144687.4(NLRP12):c.2887G>A (p.Glu963Lys)	rs139165669	0.00006
NM_144687.4(NLRP12):c.14C>A (p.Ala5Glu)	rs761545315	0.00004
NM_144687.4(NLRP12):c.153C>T (p.Ala51=)	rs757210851	0.00004
NM_144687.4(NLRP12):c.858C>T (p.Pro286=)	rs145171629	0.00003
NM_144687.4(NLRP12):c.1060C>G (p.Leu354Val)	rs1435117815	0.00001
NM_144687.4(NLRP12):c.1854C>T (p.Tyr618=)	rs142487599
NM_144687.4(NLRP12):c.2206G>A (p.Gly736Arg)	rs554602951
NM_144687.4(NLRP12):c.2830C>T (p.Arg944Trp)	rs104895570
NM_144687.4(NLRP12):c.2927+4_2927+5dup	rs763190690
NM_144687.4(NLRP12):c.3088C>G (p.Arg1030Gly)	rs201619538
NM_144687.4(NLRP12):c.882C>T (p.Asp294=)	rs147080557

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