"Ambry Genetics"[submitter] AND "KLRC3"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3115923	NM_002261.3(KLRC3):c.678+32A>G	KLRC3 (E237G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616058	NM_002261.3(KLRC3):c.678+26C>T	KLRC3 (A235V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2559961	NM_002261.3(KLRC3):c.655C>A (p.Gln219Lys)	KLRC3 (Q219K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289611	NM_002261.3(KLRC3):c.652G>C (p.Asp218His)	KLRC3 (D218H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326022	NM_002261.3(KLRC3):c.631C>T (p.His211Tyr)	KLRC3 (H211Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296211	NM_002261.3(KLRC3):c.627G>A (p.Met209Ile)	KLRC3 (M209I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115921	NM_002261.3(KLRC3):c.584A>T (p.His195Leu)	KLRC3 (H195L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2544300	NM_002261.3(KLRC3):c.443A>C (p.Lys148Thr)	KLRC3 (K148T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289106	NM_002261.3(KLRC3):c.434G>A (p.Cys145Tyr)	KLRC3 (C145Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485317	NM_002261.3(KLRC3):c.383G>A (p.Cys128Tyr)	KLRC3 (C128Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115920	NM_002261.3(KLRC3):c.334C>T (p.Arg112Cys)	KLRC3 (R112C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591569	NM_002261.3(KLRC3):c.65G>A (p.Arg22Lys)	KLRC3 (R22K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597234	NM_002261.3(KLRC3):c.58C>A (p.Gln20Lys)	KLRC3 (Q20K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance