LZTS1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052596	NM_021020.5(LZTS1):c.*10T>A	LZTS1	Single nucleotide variant (3 prime UTR variant)	LZTS1-related disorder	GBenign
Select item 2852918	NM_021020.5(LZTS1):c.1786A>T (p.Ile596Phe)	LZTS1 (I596F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3292436	NM_021020.5(LZTS1):c.1764C>T (p.Tyr588=)	LZTS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1912418	NM_021020.5(LZTS1):c.1755C>T (p.Asp585=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2180682	NM_021020.5(LZTS1):c.1750G>A (p.Ala584Thr)	LZTS1 (A584T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3012228	NM_021020.5(LZTS1):c.1749G>T (p.Gly583=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2837897	NM_021020.5(LZTS1):c.1741C>G (p.Leu581Val)	LZTS1 (L581V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003757	NM_021020.5(LZTS1):c.1729T>C (p.Leu577=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1952707	NM_021020.5(LZTS1):c.1723G>C (p.Glu575Gln)	LZTS1 (E575Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1948391	NM_021020.5(LZTS1):c.1719C>T (p.Ala573=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2233226	NM_021020.5(LZTS1):c.1717G>A (p.Ala573Thr)	LZTS1 (A573T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2707605	NM_021020.5(LZTS1):c.1716C>T (p.Ser572=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1346561	NM_021020.5(LZTS1):c.1706G>A (p.Arg569His)	LZTS1 (R569H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2724619	NM_021020.5(LZTS1):c.1705C>T (p.Arg569Cys)	LZTS1 (R569C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2177992	NM_021020.5(LZTS1):c.1702G>C (p.Ala568Pro)	LZTS1 (A568P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1670859	NM_021020.5(LZTS1):c.1699C>G (p.Leu567Val)	LZTS1 (L567V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2811524	NM_021020.5(LZTS1):c.1693C>G (p.Gln565Glu)	LZTS1 (Q565E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1674665	NM_021020.5(LZTS1):c.1680G>A (p.Leu560=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2977473	NM_021020.5(LZTS1):c.1676G>A (p.Arg559His)	LZTS1 (R559H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2513322	NM_021020.5(LZTS1):c.1675C>T (p.Arg559Cys)	LZTS1 (R559C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2007591	NM_021020.5(LZTS1):c.1668G>C (p.Arg556=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1441624	NM_021020.5(LZTS1):c.1667G>A (p.Arg556Gln)	LZTS1 (R556Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2989186	NM_021020.5(LZTS1):c.1666C>T (p.Arg556Trp)	LZTS1 (R556W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2722757	NM_021020.5(LZTS1):c.1651G>A (p.Val551Met)	LZTS1 (V551M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2420534	NM_021020.5(LZTS1):c.1650C>T (p.Tyr550=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2058857	NM_021020.5(LZTS1):c.1649A>T (p.Tyr550Phe)	LZTS1 (Y550F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3292438	NM_021020.5(LZTS1):c.1618A>G (p.Ile540Val)	LZTS1 (I540V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2915951	NM_021020.5(LZTS1):c.1612_1614del (p.Lys538del)	LZTS1 (K538del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2794474	NM_021020.5(LZTS1):c.1609_1611del (p.Glu537del)	LZTS1 (E537del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2844333	NM_021020.5(LZTS1):c.1609G>A (p.Glu537Lys)	LZTS1 (E537K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802097	NM_021020.5(LZTS1):c.1609G>C (p.Glu537Gln)	LZTS1 (E537Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1929766	NM_021020.5(LZTS1):c.1600GAG[1] (p.Glu535del)	LZTS1 (E535del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1668605	NM_021020.5(LZTS1):c.1591G>A (p.Val531Met)	LZTS1 (V531M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1935987	NM_021020.5(LZTS1):c.1586G>A (p.Arg529Gln)	LZTS1 (R529Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2136645	NM_021020.5(LZTS1):c.1585C>T (p.Arg529Trp)	LZTS1 (R529W)	Single nucleotide variant (missense variant)	LZTS1-related disorder +1 more	GUncertain significance
Select item 2134175	NM_021020.5(LZTS1):c.1585C>A (p.Arg529=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2751026	NM_021020.5(LZTS1):c.1584G>A (p.Glu528=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991157	NM_021020.5(LZTS1):c.1569G>A (p.Ser523=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2909533	NM_021020.5(LZTS1):c.1569G>C (p.Ser523=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1439756	NM_021020.5(LZTS1):c.1565C>A (p.Ser522Tyr)	LZTS1 (S522Y)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1951587	NM_021020.5(LZTS1):c.1560G>C (p.Gln520His)	LZTS1 (Q520H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1942875	NM_021020.5(LZTS1):c.1549G>A (p.Gly517Ser)	LZTS1 (G517S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2556541	NM_021020.5(LZTS1):c.1543C>T (p.Arg515Trp)	LZTS1 (R515W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2058919	NM_021020.5(LZTS1):c.1542G>A (p.Glu514=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896251	NM_021020.5(LZTS1):c.1534C>T (p.Arg512Trp)	LZTS1 (R512W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1986559	NM_021020.5(LZTS1):c.1528G>A (p.Glu510Lys)	LZTS1 (E510K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1548970	NM_021020.5(LZTS1):c.1527C>T (p.Ala509=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1903214	NM_021020.5(LZTS1):c.1523G>A (p.Arg508Gln)	LZTS1 (R508Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1450367	NM_021020.5(LZTS1):c.1517G>A (p.Arg506Gln)	LZTS1 (R506Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2875438	NM_021020.5(LZTS1):c.1516C>A (p.Arg506=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1955097	NM_021020.5(LZTS1):c.1516C>T (p.Arg506Trp)	LZTS1 (R506W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2788978	NM_021020.5(LZTS1):c.1507G>A (p.Glu503Lys)	LZTS1 (E503K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1947768	NM_021020.5(LZTS1):c.1505G>A (p.Arg502Gln)	LZTS1 (R502Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2017330	NM_021020.5(LZTS1):c.1484_1489dup (p.Asp496_Val497insGluAsp)	LZTS1	Duplication (inframe_insertion)	not provided	GUncertain significance
Select item 1574705	NM_021020.5(LZTS1):c.1489G>A (p.Val497Ile)	LZTS1 (V497I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2981295	NM_021020.5(LZTS1):c.1488C>T (p.Asp496=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1548448	NM_021020.5(LZTS1):c.1483G>A (p.Glu495Lys)	LZTS1 (E495K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1578281	NM_021020.5(LZTS1):c.1482C>T (p.Pro494=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2843616	NM_021020.5(LZTS1):c.1478T>G (p.Phe493Cys)	LZTS1 (F493C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1545756	NM_021020.5(LZTS1):c.1470G>A (p.Pro490=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1978906	NM_021020.5(LZTS1):c.1456C>T (p.Arg486Cys)	LZTS1 (R486C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3292434	NM_021020.5(LZTS1):c.1447G>A (p.Ala483Thr)	LZTS1 (A483T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2071657	NM_021020.5(LZTS1):c.1446C>T (p.Ala482=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1612143	NM_021020.5(LZTS1):c.1446C>A (p.Ala482=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2026853	NM_021020.5(LZTS1):c.1443G>C (p.Gln481His)	LZTS1 (Q481H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2006468	NM_021020.5(LZTS1):c.1438G>A (p.Ala480Thr)	LZTS1 (A480T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2973749	NM_021020.5(LZTS1):c.1418AGGAGCTGC[3] (p.Leu478_Arg479insGlnGluLeu)	LZTS1	Microsatellite (inframe_insertion)	not provided	GUncertain significance
Select item 2726605	NM_021020.5(LZTS1):c.1436G>A (p.Arg479Gln)	LZTS1 (R479Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2543518	NM_021020.5(LZTS1):c.1436G>T (p.Arg479Leu)	LZTS1 (R479L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3032783	NM_021020.5(LZTS1):c.1435C>A (p.Arg479=)	LZTS1	Single nucleotide variant (synonymous variant)	LZTS1-related disorder	GLikely benign
Select item 1514886	NM_021020.5(LZTS1):c.1431G>C (p.Glu477Asp)	LZTS1 (E477D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1244413	NM_021020.5(LZTS1):c.1423C>G (p.Leu475Val)	LZTS1 (L475V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2889361	NM_021020.5(LZTS1):c.1394G>T (p.Arg465Leu)	LZTS1 (R465L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1463113	NM_021020.5(LZTS1):c.1393C>T (p.Arg465Trp)	LZTS1 (R465W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006945	NM_021020.5(LZTS1):c.1388T>C (p.Leu463Pro)	LZTS1 (L463P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2966971	NM_021020.5(LZTS1):c.1383G>A (p.Ala461=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1908661	NM_021020.5(LZTS1):c.1382C>T (p.Ala461Val)	LZTS1 (A461V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2740794	NM_021020.5(LZTS1):c.1374G>T (p.Lys458Asn)	LZTS1 (K458N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1931795	NM_021020.5(LZTS1):c.1369A>G (p.Lys457Glu)	LZTS1 (K457E)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2908245	NM_021020.5(LZTS1):c.1366C>T (p.Arg456Cys)	LZTS1 (R456C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1919702	NM_021020.5(LZTS1):c.1342G>A (p.Glu448Lys)	LZTS1 (E448K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1909128	NM_021020.5(LZTS1):c.1335G>A (p.Leu445=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1617856	NM_021020.5(LZTS1):c.1332C>T (p.Gly444=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1601449	NM_021020.5(LZTS1):c.1331G>C (p.Gly444Ala)	LZTS1 (G444A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1568416	NM_021020.5(LZTS1):c.1323C>G (p.Arg441=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2912200	NM_021020.5(LZTS1):c.1316C>G (p.Ala439Gly)	LZTS1 (A439G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175027	NM_021020.5(LZTS1):c.1315G>A (p.Ala439Thr)	LZTS1 (A439T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1989666	NM_021020.5(LZTS1):c.1314C>T (p.Gly438=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2847602	NM_021020.5(LZTS1):c.1290G>C (p.Glu430Asp)	LZTS1 (E430D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902462	NM_021020.5(LZTS1):c.1284C>T (p.Gly428=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2727296	NM_021020.5(LZTS1):c.1276C>G (p.Leu426Val)	LZTS1 (L426V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1448776	NM_021020.5(LZTS1):c.1267C>T (p.Arg423Trp)	LZTS1 (R423W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1552749	NM_021020.5(LZTS1):c.1265C>T (p.Thr422Met)	LZTS1 (T422M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1670175	NM_021020.5(LZTS1):c.1252C>G (p.Gln418Glu)	LZTS1 (Q418E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2466166	NM_021020.5(LZTS1):c.1238T>C (p.Leu413Pro)	LZTS1 (L413P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1510096	NM_021020.5(LZTS1):c.1230C>T (p.Ser410=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2707717	NM_021020.5(LZTS1):c.1223A>G (p.Lys408Arg)	LZTS1 (K408R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1662821	NM_021020.5(LZTS1):c.1218C>T (p.Asn406=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2776309	NM_021020.5(LZTS1):c.1209G>C (p.Thr403=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2198726	NM_021020.5(LZTS1):c.1209G>A (p.Thr403=)	LZTS1	Single nucleotide variant (synonymous variant)	not provided	GBenign

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