List of variants in gene NLRP12 reported as not provided for not provided

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

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.116G>T (p.Gly39Val)	rs34436714	0.22387
NM_144687.4(NLRP12):c.1206C>G (p.Phe402Leu)	rs34971363	0.05162
NM_144687.4(NLRP12):c.289+18C>T	rs116129563	0.03610
NM_144687.4(NLRP12):c.2243+35C>T	rs104895567	0.02036
NM_144687.4(NLRP12):c.2784C>T (p.Ala928=)	rs104895569	0.01141
NM_144687.4(NLRP12):c.2701G>C (p.Val901Leu)	rs104895568	0.00265
NM_144687.4(NLRP12):c.850C>T (p.Arg284Ter)	rs104895564	0.00044
NM_144687.4(NLRP12):c.290-33G>A	rs199476242	0.00006
NM_144687.3(NLRP12):c.*544C>A	rs199475873	0.00004
NM_144687.4(NLRP12):c.1343G>C (p.Gly448Ala)	rs104895566	0.00003
NM_144687.4(NLRP12):c.1425A>G (p.Leu475=)	rs199475865	0.00001
NM_144687.4(NLRP12):c.2072+738G>T	rs199475866	0.00001
NM_144687.4(NLRP12):c.290-76A>G	rs199476241	0.00001
NM_144687.4(NLRP12):c.2072+2dup	rs104895565
NM_144687.4(NLRP12):c.2469C>A (p.Leu823=)	rs12460528
NM_144687.4(NLRP12):c.2830C>A (p.Arg944=)	rs104895570
NM_144687.4(NLRP12):c.968T>C (p.Leu323Pro)	rs199475864

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