FCF1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525293	NM_015962.5(FCF1):c.55C>G (p.Leu19Val)	FCF1 (L7V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476618	NM_015962.5(FCF1):c.65A>G (p.Gln22Arg)	FCF1 (Q10R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270517	NM_015962.5(FCF1):c.142G>A (p.Val48Ile)	FCF1 (V48I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093928	NM_015962.5(FCF1):c.144T>C (p.Val48=)	FCF1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2384600	NM_015962.5(FCF1):c.211G>A (p.Val71Ile)	FCF1 (V71I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093929	NM_015962.5(FCF1):c.218C>G (p.Thr73Ser)	FCF1 (T61S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358396	NM_015962.5(FCF1):c.259G>A (p.Val87Met)	FCF1 (V75M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093930	NM_015962.5(FCF1):c.284A>G (p.Tyr95Cys)	FCF1 (Y95C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093931	NM_015962.5(FCF1):c.298C>T (p.Pro100Ser)	FCF1 (P88S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093932	NM_015962.5(FCF1):c.389A>G (p.Glu130Gly)	FCF1 (E130G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093933	NM_015962.5(FCF1):c.455A>G (p.His152Arg)	FCF1 (H140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance