FCRL4[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278398	NM_031282.3(FCRL4):c.1544G>A (p.Ser515Asn)	FCRL4 (S515N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533629	NM_031282.3(FCRL4):c.1493C>T (p.Thr498Ile)	FCRL4 (T498I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550371	NM_031282.3(FCRL4):c.1391C>G (p.Ser464Cys)	FCRL4 (S464C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783950	NM_031282.3(FCRL4):c.1370A>G (p.Lys457Arg)	FCRL4 (K457R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3094212	NM_031282.3(FCRL4):c.1301G>T (p.Gly434Val)	FCRL4 (G434V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094211	NM_031282.3(FCRL4):c.1269C>G (p.Asp423Glu)	FCRL4 (D423E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245674	NM_031282.3(FCRL4):c.1268A>G (p.Asp423Gly)	FCRL4 (D423G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094210	NM_031282.3(FCRL4):c.1259T>C (p.Phe420Ser)	FCRL4 (F420S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278397	NM_031282.3(FCRL4):c.1255G>T (p.Gly419Cys)	FCRL4 (G419C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775612	NM_031282.3(FCRL4):c.1221G>C (p.Leu407=)	FCRL4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2621274	NM_031282.3(FCRL4):c.1123G>A (p.Val375Ile)	FCRL4 (V375I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3278396	NM_031282.3(FCRL4):c.1096G>A (p.Gly366Ser)	FCRL4 (G366S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375072	NM_031282.3(FCRL4):c.1084G>A (p.Asp362Asn)	FCRL4 (D362N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094209	NM_031282.3(FCRL4):c.1063G>C (p.Gly355Arg)	FCRL4 (G355R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551104	NM_031282.3(FCRL4):c.1046T>A (p.Ile349Asn)	FCRL4 (I349N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486600	NM_031282.3(FCRL4):c.1012C>T (p.Arg338Cys)	FCRL4 (R338C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278399	NM_031282.3(FCRL4):c.1009C>G (p.Gln337Glu)	FCRL4 (Q337E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094218	NM_031282.3(FCRL4):c.991A>G (p.Ser331Gly)	FCRL4 (S331G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535040	NM_031282.3(FCRL4):c.940G>A (p.Glu314Lys)	FCRL4 (E314K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094217	NM_031282.3(FCRL4):c.899C>T (p.Ala300Val)	FCRL4 (A300V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2374528	NM_031282.3(FCRL4):c.262C>T (p.Arg88Trp)	FCRL4 (R88W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21