List of variants in gene NLRP7 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001127255.1(NLRP7):c.-213G>T	rs199475819	0.00034
NM_001127255.2(NLRP7):c.719G>A (p.Ser240Asn)	rs199475824	0.00014
NM_001127255.2(NLRP7):c.516C>T (p.Tyr172=)	rs199475823	0.00008
NM_001127255.2(NLRP7):c.-39-4C>G	rs199476227	0.00003
NM_001127255.2(NLRP7):c.9G>A (p.Ser3=)	rs199475821	0.00003
NM_001127255.2(NLRP7):c.1171A>G (p.Thr391Ala)	rs199475827	0.00002
NM_001127255.1(NLRP7):c.-123C>T	rs199475820	0.00001
NM_001127255.2(NLRP7):c.1148C>T (p.Pro383Leu)	rs199475826	0.00001
NM_001127255.2(NLRP7):c.1235T>C (p.Leu412Pro)	rs199475828	0.00001
NM_001127255.2(NLRP7):c.1080C>A (p.Gly360=)	rs199475825
NM_001127255.2(NLRP7):c.1461G>A (p.Gly487=)	rs199475829
NM_001127255.2(NLRP7):c.1823C>T (p.Ser608Phe)	rs199475830
NM_001127255.2(NLRP7):c.446A>G (p.Asp149Gly)	rs199475822

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