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

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279720	NM_002030.5(FPR3):c.1039G>C (p.Glu347Gln)	FPR3, ZNF577 (E347Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279719	NM_002030.5(FPR3):c.55C>T (p.Pro19Ser)	FPR3, ZNF577 (P19S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3096669	NM_002030.5(FPR3):c.387T>G (p.His129Gln)	FPR3, ZNF577 (H129Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096668	NM_002030.5(FPR3):c.370T>A (p.Cys124Ser)	FPR3, ZNF577 (C124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096667	NM_002030.5(FPR3):c.278T>C (p.Phe93Ser)	FPR3, ZNF577 (F93S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096666	NM_002030.5(FPR3):c.256G>A (p.Ala86Thr)	FPR3, ZNF577 (A86T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096665	NM_002030.5(FPR3):c.104T>A (p.Val35Asp)	FPR3, ZNF577 (V35D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619344	NM_002030.5(FPR3):c.238T>C (p.Phe80Leu)	FPR3, ZNF577 (F80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495891	NM_002030.5(FPR3):c.731C>T (p.Ala244Val)	FPR3, ZNF577 (A244V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466635	NM_002030.5(FPR3):c.461T>C (p.Ile154Thr)	FPR3, ZNF577 (I154T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2403485	NM_002030.5(FPR3):c.100G>A (p.Gly34Arg)	FPR3, ZNF577 (G34R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355742	NM_002030.5(FPR3):c.509C>T (p.Thr170Met)	FPR3, ZNF577 (T170M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345627	NM_002030.5(FPR3):c.820A>T (p.Asn274Tyr)	FPR3, ZNF577 (N274Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345150	NM_002030.5(FPR3):c.70G>A (p.Val24Ile)	FPR3, ZNF577 (V24I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324568	NM_002030.5(FPR3):c.79A>T (p.Ile27Phe)	FPR3, ZNF577 (I27F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302989	NM_002030.5(FPR3):c.652A>G (p.Thr218Ala)	FPR3, ZNF577 (T218A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2251482	NM_002030.5(FPR3):c.907G>A (p.Val303Ile)	FPR3, ZNF577 (V303I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228220	NM_002030.5(FPR3):c.772G>A (p.Glu258Lys)	FPR3, ZNF577 (E258K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance