"Ambry Genetics"[submitter] AND "CLEC4C"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2546370	NM_001371390.1(CLEC4C):c.605A>G (p.Gln202Arg)	CLEC4C (Q202R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340368	NM_001371390.1(CLEC4C):c.557G>A (p.Arg186His)	CLEC4C (R149H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145670	NM_001371390.1(CLEC4C):c.556C>T (p.Arg186Cys)	CLEC4C (R155C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145669	NM_001371390.1(CLEC4C):c.484A>G (p.Asn162Asp)	CLEC4C (N131D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267692	NM_001371390.1(CLEC4C):c.449G>A (p.Arg150Gln)	CLEC4C (R119Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267694	NM_001371390.1(CLEC4C):c.431T>C (p.Leu144Pro)	CLEC4C (L144P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342372	NM_001371390.1(CLEC4C):c.229A>G (p.Ile77Val)	CLEC4C (I46V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145666	NM_001371390.1(CLEC4C):c.193C>T (p.His65Tyr)	CLEC4C (H65Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2469288	NM_001371390.1(CLEC4C):c.169A>C (p.Lys57Gln)	CLEC4C (K57Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145665	NM_001371390.1(CLEC4C):c.141G>T (p.Met47Ile)	CLEC4C (M47I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145672	NM_001371390.1(CLEC4C):c.91C>A (p.Leu31Ile)	CLEC4C (L31I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145671	NM_001371390.1(CLEC4C):c.79G>A (p.Val27Ile)	CLEC4C (V27I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145668	NM_001371390.1(CLEC4C):c.40C>T (p.Leu14Phe)	CLEC4C (L14F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145667	NM_001371390.1(CLEC4C):c.35A>G (p.Lys12Arg)	CLEC4C (K12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509065	NM_001371390.1(CLEC4C):c.4G>A (p.Val2Met)	CLEC4C (V2M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance