"Ambry Genetics"[submitter] AND "LOC126805880"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278401	NM_031281.3(FCRL5):c.2590G>A (p.Ala864Thr)	FCRL5, LOC126805880 (A864T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610398	NM_031281.3(FCRL5):c.2563G>A (p.Gly855Ser)	FCRL5, LOC126805880 (G855S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094230	NM_031281.3(FCRL5):c.2557G>A (p.Ala853Thr)	FCRL5, LOC126805880 (A853T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2561030	NM_031281.3(FCRL5):c.2544T>G (p.Phe848Leu)	FCRL5, LOC126805880 (F848L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094229	NM_031281.3(FCRL5):c.2524G>T (p.Ala842Ser)	FCRL5, LOC126805880 (A842S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458556	NM_031281.3(FCRL5):c.2518C>A (p.Leu840Met)	FCRL5, LOC126805880 (L840M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335698	NM_031281.3(FCRL5):c.2509A>G (p.Ile837Val)	FCRL5, LOC126805880 (I837V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554328	NM_031281.3(FCRL5):c.2465A>G (p.Asp822Gly)	FCRL5, LOC126805880 (D822G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094228	NM_031281.3(FCRL5):c.2431G>T (p.Ala811Ser)	FCRL5, LOC126805880 (A811S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218392	NM_031281.3(FCRL5):c.2291C>T (p.Ala764Val)	FCRL5, LOC126805880 (A764V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3278403	NM_031281.3(FCRL5):c.2284C>T (p.His762Tyr)	FCRL5, LOC126805880 (H762Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance