ClinVar Miner

List of variants in gene LZTR1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.1209C>T (p.Phe403=) rs145833752 0.00550
NM_006767.4(LZTR1):c.201-8C>T rs183476594 0.00520
NM_006767.4(LZTR1):c.2187C>T (p.Tyr729=) rs117346988 0.00222
NM_006767.4(LZTR1):c.741C>T (p.Ser247=) rs114458679 0.00183
NM_006767.4(LZTR1):c.1530C>T (p.His510=) rs190714197 0.00155
NM_006767.4(LZTR1):c.666C>T (p.Gly222=) rs35767542 0.00122
NM_006767.4(LZTR1):c.1395G>A (p.Ala465=) rs142418387 0.00108
NM_006767.4(LZTR1):c.453C>T (p.Asp151=) rs142421078 0.00069
NM_006767.4(LZTR1):c.543G>A (p.Thr181=) rs151294009 0.00063
NM_006767.4(LZTR1):c.678A>T (p.Pro226=) rs200001328 0.00021
NM_006767.4(LZTR1):c.2058C>T (p.Ala686=) rs201272562 0.00016
NM_006767.4(LZTR1):c.945C>T (p.Asp315=) rs559942119 0.00016
NM_006767.4(LZTR1):c.1194C>T (p.Asp398=) rs557960320 0.00015
NM_006767.4(LZTR1):c.263+7G>A rs185749722 0.00010
NM_006767.4(LZTR1):c.1377C>T (p.His459=) rs752985853 0.00009
NM_006767.4(LZTR1):c.2130C>T (p.Ile710=) rs149449207 0.00009
NM_006767.4(LZTR1):c.1548C>T (p.Ala516=) rs545065457 0.00008
NM_006767.4(LZTR1):c.888C>G (p.Leu296=) rs772839774 0.00008
NM_006767.4(LZTR1):c.1616-5C>T rs201238759 0.00006
NM_006767.4(LZTR1):c.1354-4G>A rs747750987 0.00005
NM_006767.4(LZTR1):c.1416G>A (p.Arg472=) rs367740343 0.00005
NM_006767.4(LZTR1):c.1943-4C>G rs368391573 0.00004
NM_006767.4(LZTR1):c.2247C>T (p.Tyr749=) rs779077819 0.00004
NM_006767.4(LZTR1):c.2274G>A (p.Ala758=) rs144870586 0.00004
NM_006767.4(LZTR1):c.138G>A (p.Gly46=) rs977844214 0.00003
NM_006767.4(LZTR1):c.489G>A (p.Thr163=) rs549102364 0.00003
NM_006767.4(LZTR1):c.2307G>A (p.Thr769=) rs201831578 0.00002
NM_006767.4(LZTR1):c.984C>T (p.Ser328=) rs374054699 0.00002
NM_006767.4(LZTR1):c.375C>A (p.Val125=) rs201356174 0.00001
NM_006767.4(LZTR1):c.1146G>C (p.Ser382=)
NM_006767.4(LZTR1):c.1191G>A (p.Ser397=)
NM_006767.4(LZTR1):c.1344G>A (p.Val448=)
NM_006767.4(LZTR1):c.1578G>A (p.Gln526=)
NM_006767.4(LZTR1):c.1941T>C (p.Ile647=)
NM_006767.4(LZTR1):c.2103C>G (p.Pro701=) rs139080986
NM_006767.4(LZTR1):c.2442G>A (p.Gln814=)
NM_006767.4(LZTR1):c.263+7_263+10del rs765081424
NM_006767.4(LZTR1):c.924C>T (p.Pro308=)

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