FCAR[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278263	NM_002000.4(FCAR):c.10A>G (p.Lys4Glu)	FCAR (K4E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510793	NM_002000.4(FCAR):c.44T>C (p.Leu15Pro)	FCAR (L15P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278260	NM_002000.4(FCAR):c.54G>C (p.Arg18Ser)	FCAR (R18S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614207	NM_002000.4(FCAR):c.75C>A (p.Asp25Glu)	FCAR (D25E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314145	NM_002000.4(FCAR):c.133G>C (p.Val45Leu)	FCAR (V33L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093912	NM_002000.4(FCAR):c.250G>C (p.Glu84Gln)	FCAR (E84Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342063	NM_002000.4(FCAR):c.259A>G (p.Ile87Val)	FCAR (I75V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348344	NM_002000.4(FCAR):c.262G>A (p.Asp88Asn)	FCAR (D76N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266794	NM_002000.4(FCAR):c.275C>T (p.Ala92Val)	FCAR (A80V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093913	NM_002000.4(FCAR):c.290G>A (p.Arg97His)	FCAR (R85H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093914	NM_002000.4(FCAR):c.310A>G (p.Ile104Val)	FCAR (I104V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461252	NM_002000.4(FCAR):c.325T>A (p.Phe109Ile)	FCAR (F109I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295115	NM_002000.4(FCAR):c.350T>A (p.Leu117Gln)	FCAR (L117Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238436	NM_002000.4(FCAR):c.371G>T (p.Gly124Val)	FCAR (G124V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555488	NM_002000.4(FCAR):c.394C>T (p.Arg132Trp)	FCAR (R120W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278264	NM_002000.4(FCAR):c.410T>C (p.Met137Thr)	FCAR (M28T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093915	NM_002000.4(FCAR):c.494C>T (p.Ser165Phe)	FCAR (S56F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300667	NM_002000.4(FCAR):c.563C>T (p.Ser188Leu)	FCAR (S176L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278262	NM_002000.4(FCAR):c.637C>T (p.Leu213Phe)	FCAR (L201F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588628	NM_002000.4(FCAR):c.671C>T (p.Thr224Met)	FCAR (T190M +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461124	NM_002000.4(FCAR):c.688C>T (p.Arg230Cys)	FCAR (R134C +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223932	NM_002000.4(FCAR):c.689G>T (p.Arg230Leu)	FCAR (R134L +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093916	NM_002000.4(FCAR):c.715G>A (p.Val239Met)	FCAR (V131M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350192	NM_002000.4(FCAR):c.733C>G (p.Leu245Val)	FCAR (L136V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261393	NM_002000.4(FCAR):c.767A>G (p.Asn256Ser)	FCAR (N160S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093917	NM_002000.4(FCAR):c.804G>T (p.Trp268Cys)	FCAR (W159C +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278261	NM_002000.4(FCAR):c.815T>C (p.Met272Thr)	FCAR (M238T +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350457	NM_002000.4(FCAR):c.842G>A (p.Arg281Gln)	FCAR (R172Q +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 28