List of variants in gene PCARE reported as benign for Retinitis pigmentosa 54

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.2112T>C (p.Asn704=)	rs10200693	0.30236
NM_001029883.3(PCARE):c.1452C>T (p.Ser484=)	rs13385188	0.29962
NM_001029883.3(PCARE):c.*27G>A	rs10182566	0.28227
NM_001029883.3(PCARE):c.1739C>T (p.Thr580Met)	rs10166913	0.16186
NM_001029883.3(PCARE):c.2374C>G (p.Leu792Val)	rs17744093	0.15871
NM_001029883.3(PCARE):c.60G>A (p.Gln20=)	rs35929540	0.15707
NM_001029883.3(PCARE):c.2499G>A (p.Pro833=)	rs34253433	0.15556
NM_001029883.3(PCARE):c.258G>A (p.Arg86=)	rs62132765	0.15123
NM_001029883.3(PCARE):c.679G>A (p.Glu227Lys)	rs114057537	0.03342
NM_001029883.3(PCARE):c.755C>A (p.Ala252Asp)	rs77003681	0.01424
NM_001029883.3(PCARE):c.2063G>A (p.Cys688Tyr)	rs149601594	0.00556
NM_001029883.3(PCARE):c.3789G>A (p.Leu1263=)	rs199689791	0.00417
NM_001029883.3(PCARE):c.3447G>A (p.Pro1149=)	rs200278694	0.00371
NM_001029883.3(PCARE):c.2875G>A (p.Ala959Thr)	rs192350796	0.00140
NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del)	rs138020654
NM_001029883.3(PCARE):c.3673_3675dupAGC

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