ClinVar Miner

List of variants in gene LZTR1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 104
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.1517C>T (p.Pro506Leu) rs763950976 0.00016
NM_006767.4(LZTR1):c.1449+3G>A rs369605093 0.00012
NM_006767.4(LZTR1):c.2428C>T (p.Arg810Trp) rs776893978 0.00009
NM_006767.4(LZTR1):c.1055A>C (p.Tyr352Ser) rs368649599 0.00006
NM_006767.4(LZTR1):c.1396C>T (p.Arg466Trp) rs550922200 0.00006
NM_006767.4(LZTR1):c.372C>T (p.Val124=) rs371891909 0.00006
NM_006767.4(LZTR1):c.1018C>T (p.Arg340Ter) rs149850248 0.00005
NM_006767.4(LZTR1):c.1785+19G>A rs777075178 0.00005
NM_006767.4(LZTR1):c.1183G>A (p.Val395Ile) rs373591504 0.00004
NM_006767.4(LZTR1):c.1433G>A (p.Arg478Gln) rs138036477 0.00004
NM_006767.4(LZTR1):c.2317G>A (p.Val773Met) rs199586863 0.00004
NM_006767.4(LZTR1):c.400+10C>T rs375186405 0.00004
NM_006767.4(LZTR1):c.946G>A (p.Val316Met) rs370315661 0.00004
NM_006767.4(LZTR1):c.1591G>A (p.Asp531Asn) rs138615487 0.00003
NM_006767.4(LZTR1):c.842C>T (p.Pro281Leu) rs1390048261 0.00003
NM_006767.4(LZTR1):c.989G>T (p.Ser330Ile) rs376331457 0.00003
NM_006767.4(LZTR1):c.1085G>A (p.Arg362Gln) rs745476291 0.00002
NM_006767.4(LZTR1):c.1175C>T (p.Ala392Val) rs767354230 0.00002
NM_006767.4(LZTR1):c.2263C>T (p.Arg755Trp) rs141161152 0.00002
NM_006767.4(LZTR1):c.2326-6T>C rs199965510 0.00002
NM_006767.4(LZTR1):c.344C>T (p.Pro115Leu) rs756852884 0.00002
NM_006767.4(LZTR1):c.1149+3A>G rs542715642 0.00001
NM_006767.4(LZTR1):c.1260+11T>A rs1298556569 0.00001
NM_006767.4(LZTR1):c.1260+3G>A rs1408575907 0.00001
NM_006767.4(LZTR1):c.1283C>T (p.Thr428Met) rs1253225013 0.00001
NM_006767.4(LZTR1):c.1354-5T>A rs368421766 0.00001
NM_006767.4(LZTR1):c.1609C>T (p.Arg537Trp) rs754507552 0.00001
NM_006767.4(LZTR1):c.1615G>A (p.Gly539Ser) rs1232362523 0.00001
NM_006767.4(LZTR1):c.1616-11C>G rs767886246 0.00001
NM_006767.4(LZTR1):c.1733_1734del (p.Asn578fs) rs1460026299 0.00001
NM_006767.4(LZTR1):c.1735G>A (p.Val579Met) rs765416902 0.00001
NM_006767.4(LZTR1):c.1842G>A (p.Met614Ile) rs763044573 0.00001
NM_006767.4(LZTR1):c.1889G>A (p.Arg630Gln) rs781776791 0.00001
NM_006767.4(LZTR1):c.1907C>T (p.Pro636Leu) rs553579098 0.00001
NM_006767.4(LZTR1):c.1934T>G (p.Val645Gly) rs1190268151 0.00001
NM_006767.4(LZTR1):c.1943-6C>A rs757311430 0.00001
NM_006767.4(LZTR1):c.1964T>C (p.Met655Thr) rs199696566 0.00001
NM_006767.4(LZTR1):c.2216C>T (p.Ser739Leu) rs762991620 0.00001
NM_006767.4(LZTR1):c.2278T>C (p.Cys760Arg) rs1419388177 0.00001
NM_006767.4(LZTR1):c.2312A>G (p.Gln771Arg) rs766983171 0.00001
NM_006767.4(LZTR1):c.2471T>C (p.Leu824Pro) rs752239353 0.00001
NM_006767.4(LZTR1):c.482del (p.Gln161fs) rs1924462309 0.00001
NM_006767.4(LZTR1):c.542C>T (p.Thr181Met) rs774992323 0.00001
NM_006767.4(LZTR1):c.589G>A (p.Ala197Thr) rs371522487 0.00001
NM_006767.4(LZTR1):c.658C>T (p.Gln220Ter) rs749437251 0.00001
NM_006767.4(LZTR1):c.1175C>A (p.Ala392Glu)
NM_006767.4(LZTR1):c.1234C>T (p.Arg412Cys) rs747430075
NM_006767.4(LZTR1):c.1235G>A (p.Arg412His) rs935736801
NM_006767.4(LZTR1):c.1339T>G (p.Phe447Val) rs1312334046
NM_006767.4(LZTR1):c.1341C>A (p.Phe447Leu) rs201016956
NM_006767.4(LZTR1):c.1373G>C (p.Gly458Ala)
NM_006767.4(LZTR1):c.1379T>C (p.Val460Ala) rs982153864
NM_006767.4(LZTR1):c.1468G>A (p.Ala490Thr)
NM_006767.4(LZTR1):c.1480A>G (p.Arg494Gly) rs2147967253
NM_006767.4(LZTR1):c.1496_1590dup (p.Asp531fs) rs1924717764
NM_006767.4(LZTR1):c.1513C>T (p.Arg505Trp) rs770974858
NM_006767.4(LZTR1):c.1561T>G (p.Phe521Val) rs1924722057
NM_006767.4(LZTR1):c.160T>G (p.Trp54Gly)
NM_006767.4(LZTR1):c.1674G>C (p.Gln558His)
NM_006767.4(LZTR1):c.1735_1785+8dup rs1924758509
NM_006767.4(LZTR1):c.1750G>A (p.Glu584Lys) rs369697241
NM_006767.4(LZTR1):c.1753_1754del (p.Ser585fs)
NM_006767.4(LZTR1):c.1764_1785+8dup rs1924760583
NM_006767.4(LZTR1):c.1785G>A (p.Lys595=)
NM_006767.4(LZTR1):c.1835T>A (p.Ile612Asn)
NM_006767.4(LZTR1):c.1862C>T (p.Ser621Phe) rs1389937904
NM_006767.4(LZTR1):c.1958A>G (p.Gln653Arg)
NM_006767.4(LZTR1):c.200G>C (p.Arg67Pro)
NM_006767.4(LZTR1):c.2070-15G>A rs1601722962
NM_006767.4(LZTR1):c.211C>T (p.His71Tyr) rs1438837277
NM_006767.4(LZTR1):c.2134G>C (p.Glu712Gln) rs1409419929
NM_006767.4(LZTR1):c.2258del (p.Asn753fs)
NM_006767.4(LZTR1):c.2378T>A (p.Leu793Gln) rs1057518130
NM_006767.4(LZTR1):c.2406+15C>T rs1350762782
NM_006767.4(LZTR1):c.2407-20C>A rs1924894264
NM_006767.4(LZTR1):c.2440_2444dup (p.Gln815fs) rs1467667029
NM_006767.4(LZTR1):c.2457CAT[1] (p.Ile821del)
NM_006767.4(LZTR1):c.2468C>T (p.Ser823Phe)
NM_006767.4(LZTR1):c.250G>C (p.Gly84Arg) rs774010552
NM_006767.4(LZTR1):c.320+13G>C
NM_006767.4(LZTR1):c.320+1G>A rs943939913
NM_006767.4(LZTR1):c.347C>T (p.Ala116Val)
NM_006767.4(LZTR1):c.352del (p.Arg118fs) rs1486960809
NM_006767.4(LZTR1):c.368C>T (p.Ala123Val)
NM_006767.4(LZTR1):c.370GTC[1] (p.Val125del) rs755783378
NM_006767.4(LZTR1):c.373G>C (p.Val125Leu)
NM_006767.4(LZTR1):c.400+1G>C rs1555927561
NM_006767.4(LZTR1):c.401-15A>C rs1924457413
NM_006767.4(LZTR1):c.401-1G>C rs747225246
NM_006767.4(LZTR1):c.428A>G (p.Asn143Ser)
NM_006767.4(LZTR1):c.436T>G (p.Leu146Val) rs1555927611
NM_006767.4(LZTR1):c.510-60_530dup rs1924491968
NM_006767.4(LZTR1):c.524G>T (p.Arg175Met) rs1924495083
NM_006767.4(LZTR1):c.578A>G (p.Tyr193Cys) rs1870169267
NM_006767.4(LZTR1):c.584G>A (p.Gly195Asp) rs777756228
NM_006767.4(LZTR1):c.594-105_594-14dup rs1924518604
NM_006767.4(LZTR1):c.652-12C>G rs1924560781
NM_006767.4(LZTR1):c.686G>C (p.Cys229Ser) rs2147964025
NM_006767.4(LZTR1):c.689A>C (p.Asn230Thr) rs752439876
NM_006767.4(LZTR1):c.714_783dup (p.Asp262delinsGlnAspValCysIleLeuTrpAlaLysArgSerGlnAsnAsnGlnGlnProLeuProValTer) rs1924566447
NM_006767.4(LZTR1):c.727T>C (p.Phe243Leu) rs2147964079
NM_006767.4(LZTR1):c.824_921dup (p.Pro308fs) rs1924610101
NM_006767.4(LZTR1):c.851G>A (p.Arg284His) rs768361273
NM_006767.4(LZTR1):c.901G>C (p.Gly301Arg)

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