Related gene-specific medical variations for Gene (Select 2359) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2619344	NM_002030.5(FPR3):c.238T>C (p.Phe80Leu)	FPR3, ZNF577 (F80L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495891	NM_002030.5(FPR3):c.731C>T (p.Ala244Val)	FPR3, ZNF577 (A244V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2466635	NM_002030.5(FPR3):c.461T>C (p.Ile154Thr)	FPR3, ZNF577 (I154T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2403485	NM_002030.5(FPR3):c.100G>A (p.Gly34Arg)	ZNF577, FPR3 (G34R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355742	NM_002030.5(FPR3):c.509C>T (p.Thr170Met)	ZNF577, FPR3 (T170M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345627	NM_002030.5(FPR3):c.820A>T (p.Asn274Tyr)	FPR3, ZNF577 (N274Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345150	NM_002030.5(FPR3):c.70G>A (p.Val24Ile)	FPR3, ZNF577 (V24I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2324568	NM_002030.5(FPR3):c.79A>T (p.Ile27Phe)	FPR3, ZNF577 (I27F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302989	NM_002030.5(FPR3):c.652A>G (p.Thr218Ala)	FPR3, ZNF577 (T218A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2251482	NM_002030.5(FPR3):c.907G>A (p.Val303Ile)	ZNF577, FPR3 (V303I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2228220	NM_002030.5(FPR3):c.772G>A (p.Glu258Lys)	ZNF577, FPR3 (E258K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance