LILRA1[gene] and "single gene"[properties] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290670	NM_006863.4(LILRA1):c.17C>A (p.Thr6Lys)	LILRA1 (T6K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508561	NM_006863.4(LILRA1):c.28T>G (p.Cys10Gly)	LILRA1 (C10G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482005	NM_006863.4(LILRA1):c.47G>A (p.Gly16Asp)	LILRA1 (G16D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321579	NM_006863.4(LILRA1):c.56C>T (p.Thr19Ile)	LILRA1 (T19I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267215	NM_006863.4(LILRA1):c.170A>G (p.Glu57Gly)	LILRA1 (E57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290663	NM_006863.4(LILRA1):c.214C>T (p.Arg72Trp)	LILRA1 (R72W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211807	NM_006863.4(LILRA1):c.224A>G (p.Gln75Arg)	LILRA1 (Q75R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336178	NM_006863.4(LILRA1):c.250C>T (p.Pro84Ser)	LILRA1 (P84S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2310548	NM_006863.4(LILRA1):c.307C>T (p.His103Tyr)	LILRA1 (H103Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118730	NM_006863.4(LILRA1):c.338C>T (p.Pro113Leu)	LILRA1 (P113L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208839	NM_006863.4(LILRA1):c.388C>A (p.Leu130Ile)	LILRA1 (L130I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251836	NM_006863.4(LILRA1):c.421G>A (p.Val141Met)	LILRA1 (V141M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556080	NM_006863.4(LILRA1):c.515C>T (p.Pro172Leu)	LILRA1 (P172L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278613	NM_006863.4(LILRA1):c.520A>G (p.Thr174Ala)	LILRA1 (T174A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118731	NM_006863.4(LILRA1):c.530G>T (p.Trp177Leu)	LILRA1 (W177L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312947	NM_006863.4(LILRA1):c.610T>C (p.Ser204Pro)	LILRA1 (S204P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118732	NM_006863.4(LILRA1):c.616C>T (p.His206Tyr)	LILRA1 (H206Y)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2589608	NM_006863.4(LILRA1):c.671A>G (p.Lys224Arg)	LILRA1 (K224R)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3290667	NM_006863.4(LILRA1):c.722G>T (p.Ser241Ile)	LILRA1 (S241I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2277960	NM_006863.4(LILRA1):c.749T>C (p.Val250Ala)	LILRA1 (V250A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2274885	NM_006863.4(LILRA1):c.887G>C (p.Arg296Thr)	LILRA1 (R296T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2378831	NM_006863.4(LILRA1):c.888A>T (p.Arg296Ser)	LILRA1 (R296S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2366123	NM_006863.4(LILRA1):c.893C>A (p.Ser298Tyr)	LILRA1 (S298Y)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2338203	NM_006863.4(LILRA1):c.895G>T (p.Gly299Cys)	LILRA1 (G299C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290669	NM_006863.4(LILRA1):c.911C>T (p.Ser304Phe)	LILRA1 (S304F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290664	NM_006863.4(LILRA1):c.917A>C (p.Glu306Ala)	LILRA1 (E306A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2240118	NM_006863.4(LILRA1):c.923C>T (p.Ser308Leu)	LILRA1 (S308L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118734	NM_006863.4(LILRA1):c.926C>G (p.Ala309Gly)	LILRA1 (A309G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2334300	NM_006863.4(LILRA1):c.936C>A (p.Asp312Glu)	LILRA1 (D312E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290672	NM_006863.4(LILRA1):c.955G>T (p.Ala319Ser)	LILRA1 (A319S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2393859	NM_006863.4(LILRA1):c.967C>T (p.Arg323Cys)	LILRA1 (R323C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2593602	NM_006863.4(LILRA1):c.986C>G (p.Ser329Trp)	LILRA1 (S329W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118735	NM_006863.4(LILRA1):c.991C>T (p.His331Tyr)	LILRA1 (H331Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290675	NM_006863.4(LILRA1):c.993T>G (p.His331Gln)	LILRA1 (H331Q)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3290666	NM_006863.4(LILRA1):c.1006G>A (p.Val336Met)	LILRA1 (V336M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118725	NM_006863.4(LILRA1):c.1007T>C (p.Val336Ala)	LILRA1 (V336A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2304035	NM_006863.4(LILRA1):c.1049G>C (p.Gly350Ala)	LILRA1 (G350A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2213609	NM_006863.4(LILRA1):c.1052C>T (p.Pro351Leu)	LILRA1 (P351L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290671	NM_006863.4(LILRA1):c.1082G>A (p.Gly361Glu)	LILRA1 (G361E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290662	NM_006863.4(LILRA1):c.1120G>A (p.Glu374Lys)	LILRA1 (E374K)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2370634	NM_006863.4(LILRA1):c.1124A>G (p.Tyr375Cys)	LILRA1 (Y375C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290665	NM_006863.4(LILRA1):c.1174T>G (p.Ser392Ala)	LILRA1 (S392A)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2373217	NM_006863.4(LILRA1):c.1175C>T (p.Ser392Leu)	LILRA1 (S392L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118726	NM_006863.4(LILRA1):c.1183T>C (p.Tyr395His)	LILRA1 (Y395H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2589192	NM_006863.4(LILRA1):c.1195G>A (p.Gly399Ser)	LILRA1 (G399S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2569805	NM_006863.4(LILRA1):c.1202T>G (p.Leu401Arg)	LILRA1 (L401R)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3290673	NM_006863.4(LILRA1):c.1205G>A (p.Ser402Asn)	LILRA1 (S402N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290674	NM_006863.4(LILRA1):c.1210A>G (p.Asn404Asp)	LILRA1 (N404D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2556079	NM_006863.4(LILRA1):c.1214C>T (p.Pro405Leu)	LILRA1 (P405L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118729	NM_006863.4(LILRA1):c.1391G>A (p.Arg464His)	LILRA1 (R464H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276095	NM_006863.4(LILRA1):c.1433T>C (p.Leu478Pro)	LILRA1 (L478P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 51