ClinVar Miner

List of variants in gene LGR5 studied for not specified

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Gene type:
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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_003667.4(LGR5):c.2021C>T (p.Thr674Met) rs148090210 0.00068
NM_003667.4(LGR5):c.640G>A (p.Val214Ile) rs148122019 0.00051
NM_003667.4(LGR5):c.1407G>C (p.Lys469Asn) rs200359280 0.00025
NM_003667.4(LGR5):c.2609C>A (p.Thr870Asn) rs145019729 0.00022
NM_003667.4(LGR5):c.1247A>G (p.Asn416Ser) rs140436677 0.00015
NM_003667.4(LGR5):c.2461A>G (p.Ile821Val) rs149958967 0.00007
NM_003667.4(LGR5):c.223A>G (p.Met75Val) rs764346723 0.00004
NM_003667.4(LGR5):c.668A>G (p.His223Arg) rs757701299 0.00004
NM_003667.4(LGR5):c.1412T>C (p.Ile471Thr) rs139824571 0.00003
NM_003667.4(LGR5):c.2182G>A (p.Ala728Thr) rs749746712 0.00003
NM_003667.4(LGR5):c.256C>A (p.Leu86Met) rs370230855 0.00003
NM_003667.4(LGR5):c.1492G>T (p.Gly498Cys) rs1033508698 0.00002
NM_003667.4(LGR5):c.1613C>T (p.Ser538Leu) rs201703093 0.00002
NM_003667.4(LGR5):c.2477A>T (p.His826Leu) rs1372193090 0.00002
NM_003667.4(LGR5):c.1328A>G (p.His443Arg) rs750353686 0.00001
NM_003667.4(LGR5):c.134G>A (p.Arg45Lys) rs1871696412 0.00001
NM_003667.4(LGR5):c.1364C>A (p.Ala455Asp) rs536797990 0.00001
NM_003667.4(LGR5):c.1466A>G (p.Tyr489Cys) rs150729317 0.00001
NM_003667.4(LGR5):c.1749C>G (p.Phe583Leu) rs771072085 0.00001
NM_003667.4(LGR5):c.2032T>C (p.Phe678Leu) rs758757228 0.00001
NM_003667.4(LGR5):c.2174A>G (p.Tyr725Cys) rs1879218439 0.00001
NM_003667.4(LGR5):c.2423T>C (p.Val808Ala) rs1879233745 0.00001
NM_003667.4(LGR5):c.2582C>A (p.Ser861Tyr) rs1263559604 0.00001
NM_003667.4(LGR5):c.2625C>A (p.Ser875Arg) rs745866493 0.00001
NM_003667.4(LGR5):c.262A>T (p.Ser88Cys) rs143081365 0.00001
NM_003667.4(LGR5):c.418C>T (p.Leu140Phe) rs1876525726 0.00001
NM_003667.4(LGR5):c.448A>C (p.Ile150Leu) rs1212398028 0.00001
NM_003667.4(LGR5):c.601A>T (p.Ile201Leu) rs768780796 0.00001
NM_003667.4(LGR5):c.654T>G (p.His218Gln) rs1877780344 0.00001
NM_003667.4(LGR5):c.656A>C (p.Asn219Thr) rs1877780526 0.00001
NM_003667.4(LGR5):c.1063C>G (p.Gln355Glu) rs2499434358
NM_003667.4(LGR5):c.1066G>A (p.Val356Met)
NM_003667.4(LGR5):c.1067T>G (p.Val356Gly)
NM_003667.4(LGR5):c.1145G>A (p.Arg382Lys) rs758187408
NM_003667.4(LGR5):c.1162G>A (p.Glu388Lys)
NM_003667.4(LGR5):c.1165A>T (p.Ile389Phe)
NM_003667.4(LGR5):c.1228A>G (p.Ile410Val)
NM_003667.4(LGR5):c.1395T>A (p.Phe465Leu) rs776281947
NM_003667.4(LGR5):c.1513G>A (p.Asp505Asn) rs750963943
NM_003667.4(LGR5):c.1546G>A (p.Ala516Thr) rs1300080811
NM_003667.4(LGR5):c.1558C>A (p.Arg520Ser) rs145133989
NM_003667.4(LGR5):c.1559G>A (p.Arg520His)
NM_003667.4(LGR5):c.1685T>C (p.Ile562Thr)
NM_003667.4(LGR5):c.1795A>G (p.Ile599Val)
NM_003667.4(LGR5):c.1813C>T (p.Leu605Phe)
NM_003667.4(LGR5):c.1822G>T (p.Val608Phe)
NM_003667.4(LGR5):c.1828A>T (p.Ser610Cys) rs2499480843
NM_003667.4(LGR5):c.1882G>A (p.Gly628Ser)
NM_003667.4(LGR5):c.1909T>C (p.Cys637Arg)
NM_003667.4(LGR5):c.2146C>T (p.Pro716Ser) rs2499482265
NM_003667.4(LGR5):c.2168T>C (p.Met723Thr)
NM_003667.4(LGR5):c.2195T>G (p.Leu732Arg)
NM_003667.4(LGR5):c.2211C>G (p.Phe737Leu) rs2137486611
NM_003667.4(LGR5):c.2404A>G (p.Lys802Glu) rs2499483295
NM_003667.4(LGR5):c.2438C>A (p.Ala813Glu)
NM_003667.4(LGR5):c.248C>T (p.Pro83Leu)
NM_003667.4(LGR5):c.2517C>T (p.Tyr839=)
NM_003667.4(LGR5):c.2561C>G (p.Ser854Cys)
NM_003667.4(LGR5):c.257T>G (p.Leu86Arg) rs149049114
NM_003667.4(LGR5):c.2593A>G (p.Thr865Ala)
NM_003667.4(LGR5):c.2645C>T (p.Pro882Leu)
NM_003667.4(LGR5):c.2656C>A (p.Pro886Thr)
NM_003667.4(LGR5):c.2663C>T (p.Pro888Leu)
NM_003667.4(LGR5):c.285A>G (p.Leu95=) rs752508501
NM_003667.4(LGR5):c.286C>T (p.Arg96Cys)
NM_003667.4(LGR5):c.353T>C (p.Val118Ala)
NM_003667.4(LGR5):c.37C>A (p.Pro13Thr) rs770233037
NM_003667.4(LGR5):c.383A>T (p.His128Leu)
NM_003667.4(LGR5):c.413G>A (p.Arg138Gln)
NM_003667.4(LGR5):c.417C>A (p.Ser139Arg) rs779090996
NM_003667.4(LGR5):c.429G>A (p.Leu143=)
NM_003667.4(LGR5):c.667C>T (p.His223Tyr)
NM_003667.4(LGR5):c.702C>G (p.His234Gln)
NM_003667.4(LGR5):c.854C>T (p.Thr285Ile)
NM_003667.4(LGR5):c.92T>C (p.Leu31Pro)

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