Related gene-specific medical variations for Gene (Select 79368) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278383	NM_030764.4(FCRL2):c.321A>T (p.Gln107His)	FCRL2, LOC126805883 (Q107H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094184	NM_030764.4(FCRL2):c.71C>T (p.Ala24Val)	FCRL2, LOC126805883 (A24V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094183	NM_030764.4(FCRL2):c.298A>G (p.Ile100Val)	FCRL2, LOC126805883 (I100V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094181	NM_030764.4(FCRL2):c.193T>C (p.Ser65Pro)	FCRL2, LOC126805883 (S65P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094180	NM_030764.4(FCRL2):c.162T>A (p.Asp54Glu)	FCRL2, LOC126805883 (D54E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591074	NM_030764.4(FCRL2):c.499G>T (p.Val167Leu)	FCRL2, LOC126805883 (V167L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569956	NM_030764.4(FCRL2):c.87C>A (p.Phe29Leu)	FCRL2, LOC126805883 (F29L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559168	NM_030764.4(FCRL2):c.392G>A (p.Arg131Gln)	FCRL2, LOC126805883 (R131Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2461220	NM_030764.4(FCRL2):c.329T>C (p.Val110Ala)	FCRL2, LOC126805883 (V110A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333297	NM_030764.4(FCRL2):c.77C>T (p.Ser26Phe)	FCRL2, LOC126805883 (S26F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329548	NM_030764.4(FCRL2):c.73C>T (p.Pro25Ser)	FCRL2, LOC126805883 (P25S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258075	NM_030764.4(FCRL2):c.337G>A (p.Ala113Thr)	FCRL2, LOC126805883 (A113T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234538	NM_030764.4(FCRL2):c.92G>A (p.Gly31Glu)	FCRL2, LOC126805883 (G31E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208346	NM_030764.4(FCRL2):c.322C>T (p.Arg108Cys)	FCRL2, LOC126805883 (R108C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance