"Clinical Genetics, Academic Medical Center"[submitter] AND "MERTK"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 330741	NM_006343.3(MERTK):c.102A>G (p.Leu34=)	MERTK	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 775751	NM_006343.3(MERTK):c.107C>T (p.Pro36Leu)	MERTK (P36L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1064335	NM_006343.3(MERTK):c.1058C>T (p.Ala353Val)	MERTK, LOC112806037 (A353V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 330752	NM_006343.3(MERTK):c.1261C>T (p.Arg421Trp)	MERTK (R421W)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1050926	NM_006343.3(MERTK):c.1340G>A (p.Arg447Gln)	MERTK (R447Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 784993	NM_006343.3(MERTK):c.1353A>G (p.Gln451=)	MERTK	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 330763	NM_006343.3(MERTK):c.1960+8C>T	MERTK	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 194960	NM_006343.3(MERTK):c.2593C>T (p.Arg865Trp)	MERTK (R865W)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 38 +3 more	GConflicting classifications of pathogenicity

ClinVar