"Fulgent Genetics, Fulgent Genetics"[submitter] AND "PCARE"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 785849	NM_001029883.3(PCARE):c.3522C>T (p.Asp1174=)	PCARE	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 54 +2 more	GBenign/Likely benign
Select item 283187	NM_001029883.3(PCARE):c.3447G>A (p.Pro1149=)	PCARE	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +3 more	GBenign/Likely benign
Select item 193142	NM_001029883.3(PCARE):c.3058_3059delinsAG (p.Gln1020Arg)	PCARE (Q1020R)	Indel (missense variant)	Retinitis pigmentosa 54 +2 more	GBenign/Likely benign
Select item 857282	NM_001029883.3(PCARE):c.3029G>A (p.Arg1010Gln)	PCARE (R1010Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 335652	NM_001029883.3(PCARE):c.1968G>T (p.Arg656Ser)	PCARE (R656S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 335664	NM_001029883.3(PCARE):c.1297C>T (p.Pro433Ser)	PCARE (P433S)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 54 +3 more	GConflicting classifications of pathogenicity
Select item 854244	NM_001029883.3(PCARE):c.8G>A (p.Cys3Tyr)	PCARE (C3Y)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 54 +2 more	GConflicting classifications of pathogenicity

ClinVar