List of variants in gene NLRP14 reported as benign by GeneDx

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_176822.4(NLRP14):c.143A>C (p.Asn48Thr)	rs12801277	0.96856
NM_176822.4(NLRP14):c.498C>T (p.Phe166=)	rs7123944	0.95835
NM_176822.4(NLRP14):c.2253G>A (p.Glu751=)	rs1552726	0.93922
NM_176822.4(NLRP14):c.362-320T>C	rs10160530	0.70443
NC_000011.10:g.7071602A>G	rs10839711	0.70191
NM_176822.4(NLRP14):c.3146+85C>A	rs10769763	0.64668
NM_176822.4(NLRP14):c.289+131del	rs11288450	0.61826
NM_176822.4(NLRP14):c.2462+183A>G	rs10500676	0.61592
NM_176822.4(NLRP14):c.2124-36G>A	rs1552727	0.58005
NM_176822.4(NLRP14):c.2124-179G>T	rs10839700	0.57141
NM_176822.4(NLRP14):c.1959-198G>T	rs7109723	0.56434
NM_176822.4(NLRP14):c.2634-254T>G	rs10839709	0.54569
NM_176822.4(NLRP14):c.2422G>A (p.Glu808Lys)	rs10839708	0.54446
NM_176822.4(NLRP14):c.164G>A (p.Arg55Gln)	rs61063081	0.15385
NM_176822.4(NLRP14):c.3028C>T (p.Leu1010Phe)	rs17280682	0.15054
NM_176822.4(NLRP14):c.-21-48T>A	rs17279697	0.09860
NM_176822.4(NLRP14):c.2292-104A>C	rs16921939	0.07629
NM_176822.4(NLRP14):c.2804+125_2804+128del	rs138550484	0.06456
NM_176822.4(NLRP14):c.1200T>C (p.Phe400=)	rs76429148	0.06204
NM_176822.4(NLRP14):c.2976-111A>C	rs80332896	0.05336
NM_176822.4(NLRP14):c.361+46T>G	rs17194742	0.04527
NM_176822.4(NLRP14):c.2124-272T>C	rs72849553	0.03954
NM_176822.4(NLRP14):c.2463-172C>T	rs79694361	0.03733
NM_176822.4(NLRP14):c.275A>G (p.Lys92Arg)	rs16921697	0.03403
NM_176822.4(NLRP14):c.290-275A>T	rs76261649	0.02730
NM_176822.4(NLRP14):c.322A>T (p.Lys108Ter)	rs76274604	0.00521
NM_176822.4(NLRP14):c.1958+74C>A	rs6578821
NM_176822.4(NLRP14):c.2123+105C>T	rs75044836
NM_176822.4(NLRP14):c.2124-244A>T	rs4439493
NM_176822.4(NLRP14):c.2805-305A>G	rs1907613
NM_176822.4(NLRP14):c.289+262_289+275del	rs60100976
NM_176822.4(NLRP14):c.2976-160A>C	rs10769762
NM_176822.4(NLRP14):c.362-322A>G	rs10160485

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