List of variants in gene NLRP12 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.910C>T (p.His304Tyr)	rs141245482	0.00392
NM_144687.4(NLRP12):c.779C>T (p.Thr260Met)	rs150280940	0.00027
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.665G>A (p.Gly222Asp)	rs371385297	0.00002
NM_144687.4(NLRP12):c.3174C>A (p.Asp1058Glu)	rs1690166860	0.00001
NM_144687.4(NLRP12):c.-18G>A	rs781775783
NM_144687.4(NLRP12):c.1538del (p.Ile513fs)	rs903100692
NM_144687.4(NLRP12):c.1587C>G (p.Asp529Glu)	rs781712648
NM_144687.4(NLRP12):c.2072+2dup	rs104895565

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