"Ambry Genetics"[submitter] AND "FCMR"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3094140	NM_005449.5(FCMR):c.1166C>T (p.Pro389Leu)	FCMR, LOC126805991 (P230L +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222450	NM_005449.5(FCMR):c.1128G>C (p.Met376Ile)	FCMR, LOC126805991 (M220I +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522729	NM_005449.5(FCMR):c.1123G>A (p.Ala375Thr)	FCMR, LOC126805991 (A216T +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2384470	NM_005449.5(FCMR):c.1009G>A (p.Gly337Ser)	FCMR (G187S +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094139	NM_005449.5(FCMR):c.1006C>G (p.Pro336Ala)	FCMR (P177A +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266378	NM_005449.5(FCMR):c.1003G>A (p.Val335Ile)	FCMR (V179I +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094148	NM_005449.5(FCMR):c.975G>A (p.Ala325=)	FCMR (G282R)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 3094147	NM_005449.5(FCMR):c.974C>G (p.Ala325Gly)	FCMR (A175G +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456215	NM_005449.5(FCMR):c.922C>A (p.Pro308Thr)	FCMR (P152T +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461918	NM_005449.5(FCMR):c.902G>T (p.Arg301Met)	FCMR (R151M +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094145	NM_005449.5(FCMR):c.882C>T (p.Arg294=)	FCMR (R251C)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2307850	NM_005449.5(FCMR):c.794T>C (p.Leu265Pro)	FCMR (L115P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365749	NM_005449.5(FCMR):c.760A>T (p.Ile254Phe)	FCMR (I173F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407436	NM_005449.5(FCMR):c.705G>T (p.Arg235Ser)	FCMR (R154S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472122	NM_005449.5(FCMR):c.605G>A (p.Arg202Gln)	FCMR (R202Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398716	NM_005449.5(FCMR):c.593G>A (p.Gly198Asp)	FCMR (G117D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303332	NM_005449.5(FCMR):c.496C>A (p.Pro166Thr)	FCMR (P166T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312422	NM_005449.5(FCMR):c.482C>A (p.Thr161Asn)	FCMR (T161N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613254	NM_005449.5(FCMR):c.442T>C (p.Phe148Leu)	FCMR (F148L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3094143	NM_005449.5(FCMR):c.421T>C (p.Trp141Arg)	FCMR (W29R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330536	NM_005449.5(FCMR):c.409G>C (p.Glu137Gln)	FCMR (E137Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380953	NM_005449.5(FCMR):c.379G>A (p.Glu127Lys)	FCMR (E46K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589263	NM_005449.5(FCMR):c.368A>G (p.His123Arg)	FCMR (H154R +1 more)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 3094142	NM_005449.5(FCMR):c.337G>A (p.Gly113Arg)	FCMR (G113R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334593	NM_005449.5(FCMR):c.253A>C (p.Asn85His)	FCMR (N116H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094141	NM_005449.5(FCMR):c.248G>A (p.Arg83His)	FCMR (R114H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2375330	NM_005449.5(FCMR):c.221G>A (p.Gly74Asp)	FCMR (G74D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518675	NM_005449.5(FCMR):c.209C>T (p.Ala70Val)	FCMR (A70V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2214283	NM_005449.5(FCMR):c.149G>A (p.Arg50Gln)	FCMR (R50Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517181	NM_005449.5(FCMR):c.134G>A (p.Arg45Lys)	FCMR (R76K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094146	NM_005449.5(FCMR):c.91G>C (p.Gly31Arg)	FCMR (G62R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265417	NM_005449.5(FCMR):c.78G>T (p.Glu26Asp)	FCMR (E57D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409662	NM_005449.5(FCMR):c.64G>A (p.Glu22Lys)	FCMR (E53K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300550	NM_005449.5(FCMR):c.62C>G (p.Pro21Arg)	FCMR (P21R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 34