"Ambry Genetics"[submitter] AND "FCGR3B"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3094079	NM_001244753.2(FCGR3B):c.680T>A (p.Phe227Tyr)	FCGR3B (F124Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601510	NM_001244753.2(FCGR3B):c.649C>G (p.Leu217Val)	FCGR3B (L114V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281791	NM_001244753.2(FCGR3B):c.583G>A (p.Ala195Thr)	FCGR3B (A194T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260093	NM_001244753.2(FCGR3B):c.576A>C (p.Gln192His)	FCGR3B (Q191H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331969	NM_001244753.2(FCGR3B):c.502G>A (p.Gly168Ser)	FCGR3B (G168S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094078	NM_001244753.2(FCGR3B):c.484G>A (p.Ala162Thr)	FCGR3B (A145T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094077	NM_001244753.2(FCGR3B):c.472C>T (p.His158Tyr)	FCGR3B (H157Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2348670	NM_001244753.2(FCGR3B):c.412A>G (p.Lys138Glu)	FCGR3B (K137E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558946	NM_001244753.2(FCGR3B):c.410A>C (p.His137Pro)	FCGR3B (H137P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278339	NM_001244753.2(FCGR3B):c.368C>T (p.Pro123Leu)	FCGR3B (P106L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235672	NM_001244753.2(FCGR3B):c.296C>T (p.Pro99Leu)	FCGR3B (P99L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507872	NM_001244753.2(FCGR3B):c.290G>A (p.Ser97Asn)	FCGR3B (S80N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094076	NM_001244753.2(FCGR3B):c.249C>G (p.Asp83Glu)	FCGR3B (D66E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543493	NM_001244753.2(FCGR3B):c.235G>A (p.Ala79Thr)	FCGR3B (A79T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278340	NM_001244753.2(FCGR3B):c.206G>A (p.Ser69Asn)	FCGR3B (S69N +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3278338	NM_001244753.2(FCGR3B):c.196C>T (p.Leu66Phe)	FCGR3B (L49F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094075	NM_001244753.2(FCGR3B):c.170C>T (p.Ser57Phe)	FCGR3B (S40F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287278	NM_001244753.2(FCGR3B):c.167A>G (p.Asn56Ser)	FCGR3B (N55S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347687	NM_001244753.2(FCGR3B):c.79G>C (p.Val27Leu)	FCGR3B (V10L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354537	NM_001244753.2(FCGR3B):c.53T>C (p.Met18Thr)	FCGR3B (M18T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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Items: 20