CFLAR[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2558183	NM_003879.7(CFLAR):c.22C>G (p.Gln8Glu)	CFLAR (Q8E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2480008	NM_003879.7(CFLAR):c.58A>G (p.Met20Val)	CFLAR (M20V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2468002	NM_003879.7(CFLAR):c.354T>G (p.Asp118Glu)	CFLAR (D22E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454640	NM_003879.7(CFLAR):c.360G>A (p.Met120Ile)	CFLAR (M120I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268192	NM_003879.7(CFLAR):c.944G>A (p.Arg315Gln)	CFLAR (R219Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3143839	NM_003879.7(CFLAR):c.1021A>G (p.Met341Val)	CFLAR (M341V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307107	NM_003879.7(CFLAR):c.1099C>G (p.Leu367Val)	CFLAR (L332V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773850	NM_003879.7(CFLAR):c.1125G>A (p.Val375=)	CFLAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2382687	NM_003879.7(CFLAR):c.1145A>G (p.Asn382Ser)	CFLAR (N137S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3143840	NM_003879.7(CFLAR):c.1190G>C (p.Arg397Pro)	CFLAR (R152P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance