"Ambry Genetics"[submitter] AND "FCRLB"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2553029	NM_001002901.4(FCRLB):c.91T>G (p.Trp31Gly)	FCRLB (W24G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596702	NM_001002901.4(FCRLB):c.222C>A (p.Ser74Arg)	FCRLB (S74R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554376	NM_001002901.4(FCRLB):c.404T>C (p.Leu135Pro)	FCRLB (L135P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326127	NM_001002901.4(FCRLB):c.646G>A (p.Val216Met)	FCRLB, LOC129931781 (V216M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2356833	NM_001002901.4(FCRLB):c.673C>T (p.Pro225Ser)	FCRLB, LOC129931781 (P225S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2260534	NM_001002901.4(FCRLB):c.679A>G (p.Lys227Glu)	LOC129931781, FCRLB (E192G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2254505	NM_001002901.4(FCRLB):c.700T>A (p.Phe234Ile)	FCRLB, LOC129931781 (V192D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2285231	NM_001002901.4(FCRLB):c.703G>T (p.Ala235Ser)	FCRLB (R200L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2333567	NM_001002901.4(FCRLB):c.752A>G (p.Glu251Gly)	FCRLB, LOC129931782 (E251G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2288939	NM_001002901.4(FCRLB):c.863C>A (p.Pro288Gln)	FCRLB, LOC129931783 (P288Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2525550	NM_001002901.4(FCRLB):c.923C>T (p.Ala308Val)	FCRLB (L253F +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2392720	NM_001002901.4(FCRLB):c.944C>T (p.Ser315Phe)	FCRLB (P267S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2474657	NM_001002901.4(FCRLB):c.1001C>G (p.Thr334Ser)	FCRLB (P279A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2480905	NM_001002901.4(FCRLB):c.1210A>C (p.Thr404Pro)	FCRLB (T404P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220526	NM_001002901.4(FCRLB):c.1211C>T (p.Thr404Met)	FCRLB (T404M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2376119	NM_001002901.4(FCRLB):c.1225A>G (p.Thr409Ala)	FCRLB (T409A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2356499	NM_001002901.4(FCRLB):c.1247C>G (p.Pro416Arg)	FCRLB (P416R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance