"Ambry Genetics"[submitter] AND "LRP3"[gene] - ClinVar

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Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2470795	NM_002333.4(LRP3):c.89C>T (p.Thr30Ile)	LRP3 (T30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120275	NM_002333.4(LRP3):c.107C>T (p.Ala36Val)	LRP3 (A36V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120277	NM_002333.4(LRP3):c.122C>T (p.Ala41Val)	LRP3 (A41V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605330	NM_002333.4(LRP3):c.158G>A (p.Arg53Gln)	LRP3 (R53Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523670	NM_002333.4(LRP3):c.194A>G (p.Asn65Ser)	LRP3 (N65S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120285	NM_002333.4(LRP3):c.200C>T (p.Pro67Leu)	LRP3 (P67L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217890	NM_002333.4(LRP3):c.269A>G (p.Asn90Ser)	LRP3 (N90S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120288	NM_002333.4(LRP3):c.367G>A (p.Ala123Thr)	LRP3 (A123T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405515	NM_002333.4(LRP3):c.379G>A (p.Ala127Thr)	LRP3 (A127T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209490	NM_002333.4(LRP3):c.418C>T (p.His140Tyr)	LRP3 (H140Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390958	NM_002333.4(LRP3):c.439G>A (p.Gly147Ser)	LRP3 (G147S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488315	NM_002333.4(LRP3):c.458G>A (p.Arg153His)	LRP3 (R153H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549711	NM_002333.4(LRP3):c.472C>G (p.Arg158Gly)	LOC132090548, LRP3 (R158G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120290	NM_002333.4(LRP3):c.602C>T (p.Ser201Leu)	LRP3 (S201L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596691	NM_002333.4(LRP3):c.605C>T (p.Ala202Val)	LRP3 (A202V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291431	NM_002333.4(LRP3):c.661G>A (p.Gly221Arg)	LRP3 (G221R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404345	NM_002333.4(LRP3):c.667C>T (p.Arg223Cys)	LRP3 (R223C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590597	NM_002333.4(LRP3):c.697C>T (p.Arg233Cys)	LRP3 (R233C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546165	NM_002333.4(LRP3):c.698G>A (p.Arg233His)	LRP3 (R233H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120291	NM_002333.4(LRP3):c.754C>A (p.Leu252Met)	LRP3 (L252M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120292	NM_002333.4(LRP3):c.758C>T (p.Ala253Val)	LRP3 (A253V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120293	NM_002333.4(LRP3):c.860A>G (p.Asp287Gly)	LRP3 (D287G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206807	NM_002333.4(LRP3):c.889C>A (p.Gln297Lys)	LRP3 (Q297K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492565	NM_002333.4(LRP3):c.971C>T (p.Thr324Met)	LRP3 (T324M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120274	NM_002333.4(LRP3):c.1000G>A (p.Val334Met)	LRP3 (V334M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291430	NM_002333.4(LRP3):c.1015G>A (p.Ala339Thr)	LRP3 (A339T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491050	NM_002333.4(LRP3):c.1051G>A (p.Ala351Thr)	LRP3 (A351T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600695	NM_002333.4(LRP3):c.1054C>T (p.Arg352Cys)	LRP3 (R352C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338348	NM_002333.4(LRP3):c.1108C>T (p.Pro370Ser)	LRP3 (P370S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239698	NM_002333.4(LRP3):c.1109C>T (p.Pro370Leu)	LRP3 (P370L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120276	NM_002333.4(LRP3):c.1162G>A (p.Asp388Asn)	LRP3 (D388N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360761	NM_002333.4(LRP3):c.1234G>A (p.Gly412Ser)	LRP3 (G412S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515773	NM_002333.4(LRP3):c.1270G>A (p.Glu424Lys)	LRP3 (E424K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548985	NM_002333.4(LRP3):c.1273G>C (p.Gly425Arg)	LRP3 (G425R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249010	NM_002333.4(LRP3):c.1277G>A (p.Gly426Asp)	LRP3 (G426D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240910	NM_002333.4(LRP3):c.1295C>T (p.Thr432Met)	LRP3 (T432M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239699	NM_002333.4(LRP3):c.1380C>G (p.Phe460Leu)	LRP3 (F460L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291433	NM_002333.4(LRP3):c.1382A>G (p.His461Arg)	LRP3 (H461R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598189	NM_002333.4(LRP3):c.1456G>A (p.Glu486Lys)	LRP3 (E486K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378590	NM_002333.4(LRP3):c.1460A>G (p.His487Arg)	LRP3 (H487R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120278	NM_002333.4(LRP3):c.1474G>A (p.Ala492Thr)	LRP3 (A492T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214771	NM_002333.4(LRP3):c.1480C>T (p.Pro494Ser)	LRP3 (P494S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291432	NM_002333.4(LRP3):c.1483C>T (p.Arg495Cys)	LRP3 (R495C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401862	NM_002333.4(LRP3):c.1493T>C (p.Ile498Thr)	LRP3 (I498T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478441	NM_002333.4(LRP3):c.1523G>A (p.Cys508Tyr)	LRP3 (C508Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2563564	NM_002333.4(LRP3):c.1580C>T (p.Thr527Met)	LRP3 (T527M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375865	NM_002333.4(LRP3):c.1585G>C (p.Glu529Gln)	LRP3 (E529Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408425	NM_002333.4(LRP3):c.1615C>T (p.Arg539Cys)	LRP3 (R539C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120280	NM_002333.4(LRP3):c.1636C>T (p.Arg546Trp)	LRP3 (R546W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291429	NM_002333.4(LRP3):c.1720T>C (p.Ser574Pro)	LRP3 (S574P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507978	NM_002333.4(LRP3):c.1730C>T (p.Ser577Phe)	LRP3 (S577F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253108	NM_002333.4(LRP3):c.1748G>T (p.Arg583Leu)	LRP3 (R583L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371975	NM_002333.4(LRP3):c.1759C>T (p.Arg587Trp)	LRP3 (R587W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364313	NM_002333.4(LRP3):c.1760G>A (p.Arg587Gln)	LRP3 (R587Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283503	NM_002333.4(LRP3):c.1774C>T (p.Arg592Trp)	LRP3 (R592W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120281	NM_002333.4(LRP3):c.1790G>A (p.Arg597Gln)	LRP3 (R597Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207544	NM_002333.4(LRP3):c.1801C>T (p.Arg601Cys)	LRP3 (R601C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395944	NM_002333.4(LRP3):c.1808G>A (p.Arg603His)	LRP3 (R603H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404991	NM_002333.4(LRP3):c.1844C>T (p.Pro615Leu)	LRP3 (P615L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208577	NM_002333.4(LRP3):c.1856G>A (p.Arg619Gln)	LRP3 (R619Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120282	NM_002333.4(LRP3):c.1886G>A (p.Arg629His)	LRP3 (R629H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521840	NM_002333.4(LRP3):c.1947C>G (p.Asp649Glu)	LRP3 (D649E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239671	NM_002333.4(LRP3):c.1990G>A (p.Gly664Arg)	LRP3 (G664R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120283	NM_002333.4(LRP3):c.2003C>G (p.Pro668Arg)	LRP3 (P668R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404090	NM_002333.4(LRP3):c.2014G>A (p.Gly672Ser)	LRP3 (G672S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3291434	NM_002333.4(LRP3):c.2054C>T (p.Pro685Leu)	LRP3 (P685L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120286	NM_002333.4(LRP3):c.2153G>A (p.Arg718Gln)	LRP3 (R718Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343784	NM_002333.4(LRP3):c.2272A>G (p.Met758Val)	LRP3 (M758V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120287	NM_002333.4(LRP3):c.2287G>A (p.Asp763Asn)	LRP3 (D763N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213243	NM_002333.4(LRP3):c.2290G>C (p.Asp764His)	LRP3 (D764H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 70