"Ambry Genetics"[submitter] AND "LOC126862931"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2624064	NM_001080978.4(LILRB2):c.641T>A (p.Leu214Gln)	LILRB2, LOC126862931 (L214Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350707	NM_001080978.4(LILRB2):c.641T>C (p.Leu214Pro)	LILRB2, LOC126862931 (L214P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118794	NM_001080978.4(LILRB2):c.625T>C (p.Ser209Pro)	LILRB2, LOC126862931 (S93P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366526	NM_001080978.4(LILRB2):c.614A>G (p.Tyr205Cys)	LILRB2, LOC126862931 (Y205C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290708	NM_001080978.4(LILRB2):c.602T>C (p.Leu201Ser)	LOC126862931, LILRB2 (L201S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2407213	NM_001080978.4(LILRB2):c.593G>C (p.Gly198Ala)	LILRB2, LOC126862931 (G198A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388414	NM_001080978.4(LILRB2):c.586T>A (p.Cys196Ser)	LILRB2, LOC126862931 (C196S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400879	NM_001080978.4(LILRB2):c.580C>T (p.His194Tyr)	LILRB2, LOC126862931 (H194Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2400885	NM_001080978.4(LILRB2):c.578C>G (p.Ser193Trp)	LILRB2, LOC126862931 (S193W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118793	NM_001080978.4(LILRB2):c.569G>A (p.Arg190His)	LILRB2, LOC126862931 (R190H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3290700	NM_001080978.4(LILRB2):c.566A>G (p.Asn189Ser)	LILRB2, LOC126862931 (N189S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3118792	NM_001080978.4(LILRB2):c.562C>T (p.Pro188Ser)	LILRB2, LOC126862931 (P188S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457843	NM_001080978.4(LILRB2):c.556G>A (p.Val186Met)	LILRB2, LOC126862931 (V186M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386949	NM_001080978.4(LILRB2):c.535G>C (p.Ala179Pro)	LILRB2, LOC126862931 (A179P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346599	NM_001080978.4(LILRB2):c.521G>A (p.Arg174His)	LILRB2, LOC126862931 (R58H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3290711	NM_001080978.4(LILRB2):c.454G>A (p.Gly152Ser)	LILRB2, LOC126862931 (G36S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511415	NM_001080978.4(LILRB2):c.401T>G (p.Val134Gly)	LILRB2, LOC126862931 (V134G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370405	NM_001080978.4(LILRB2):c.393C>A (p.Ser131Arg)	LILRB2, LOC126862931 (S131R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306206	NM_001080978.4(LILRB2):c.388C>T (p.Pro130Ser)	LILRB2, LOC126862931 (P130S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290713	NM_001080978.4(LILRB2):c.374C>T (p.Thr125Ile)	LILRB2, LOC126862931 (T9I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293919	NM_001080978.4(LILRB2):c.341T>G (p.Val114Gly)	LILRB2, LOC126862931 (V114G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2372306	NM_001080978.4(LILRB2):c.262A>G (p.Ile88Val)	LILRB2, LOC126862931 (I88V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2330149	NM_001080978.4(LILRB2):c.233T>G (p.Val78Gly)	LILRB2, LOC126862931 (V78G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290712	NM_001080978.4(LILRB2):c.223C>T (p.Pro75Ser)	LILRB2, LOC126862931 (P75S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2267458	NM_001080978.4(LILRB2):c.215G>A (p.Arg72Gln)	LILRB2, LOC126862931 (R72Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290706	NM_001080978.4(LILRB2):c.214C>T (p.Arg72Trp)	LILRB2, LOC126862931 (R72W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2280175	NM_001080978.4(LILRB2):c.191A>G (p.Lys64Arg)	LILRB2, LOC126862931 (K64R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2620785	NM_001080978.4(LILRB2):c.121C>A (p.Gln41Lys)	LILRB2, LOC126862931 (Q41K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290704	NM_001080978.4(LILRB2):c.119C>T (p.Thr40Ile)	LILRB2, LOC126862931 (T40I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 29