List of variants in gene NLRP14 reported by Human Evolutionary Genetics, Institut Pasteur

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_176822.4(NLRP14):c.289+28G>A	rs199475880	0.00067
NM_176822.4(NLRP14):c.2805-162C>T	rs199475887	0.00027
NM_176822.4(NLRP14):c.3147-109T>C	rs199475891	0.00022
NM_176822.4(NLRP14):c.3146+24G>C	rs199475890	0.00012
NM_176822.4(NLRP14):c.2066C>G (p.Ala689Gly)	rs199475884	0.00003
NM_176822.4(NLRP14):c.3049A>T (p.Ile1017Leu)	rs199475889	0.00002
NM_176822.4(NLRP14):c.*55G>C	rs199475892	0.00001
NM_176822.4(NLRP14):c.2027G>C (p.Arg676Thr)	rs199475883	0.00001
NM_176822.4(NLRP14):c.2291+112T>A	rs199475885	0.00001
NM_176822.4(NLRP14):c.1282_1283del (p.Cys428fs)	rs199476260
NM_176822.4(NLRP14):c.1976C>T (p.Thr659Ile)	rs199475882
NM_176822.4(NLRP14):c.2633+52T>C	rs199475886
NM_176822.4(NLRP14):c.2976-24A>G	rs199475888
NM_176822.4(NLRP14):c.609C>A (p.Gly203=)	rs199475881

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