List of variants in gene NLRP4 reported as not provided

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_134444.4(NLRP4):c.*283T>C	rs199475756	0.00318
NM_134444.5(NLRP4):c.2019-215T>C	rs199475749	0.00140
NM_134444.5(NLRP4):c.1856+50C>T	rs199475747	0.00111
NM_134444.5(NLRP4):c.2697-194C>G	rs199475753	0.00063
NM_134444.5(NLRP4):c.-175G>A	rs199475742	0.00004
NM_134444.5(NLRP4):c.1857-68G>A	rs199475748	0.00002
NM_134444.5(NLRP4):c.*164T>A	rs199475755
NM_134444.5(NLRP4):c.-275T>G	rs199475741
NM_134444.5(NLRP4):c.-66+6G>T	rs199475743
NM_134444.5(NLRP4):c.-66+7G>T	rs199475744
NM_134444.5(NLRP4):c.2143T>G (p.Cys715Gly)	rs199475750
NM_134444.5(NLRP4):c.2178A>G (p.Lys726=)	rs199475751
NM_134444.5(NLRP4):c.2187-56G>C	rs199475752
NM_134444.5(NLRP4):c.2697-169A>G	rs199475754
NM_134444.5(NLRP4):c.446_447insA (p.Thr150fs)	rs199475745
NM_134444.5(NLRP4):c.457_466del (p.Ile153fs)	rs199476224
NM_134444.5(NLRP4):c.583G>C (p.Glu195Gln)	rs199475746

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