ClinVar Miner

Variants in gene LZTR1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 35
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.2187C>T (p.Tyr729=) rs117346988 0.00222
NM_006767.4(LZTR1):c.1530C>T (p.His510=) rs190714197 0.00155
NM_006767.4(LZTR1):c.1904C>T (p.Pro635Leu) rs148677674 0.00077
NM_006767.4(LZTR1):c.1990G>A (p.Ala664Thr) rs140874089 0.00072
NM_006767.4(LZTR1):c.1723G>A (p.Asp575Asn) rs139368531 0.00061
NM_006767.4(LZTR1):c.652-10C>A rs200169897 0.00049
NM_006767.4(LZTR1):c.1531G>A (p.Val511Met) rs200062851 0.00046
NM_006767.4(LZTR1):c.2190C>T (p.Gly730=) rs144092577 0.00034
NM_006767.4(LZTR1):c.1939A>G (p.Ile647Val) rs148916790 0.00025
NM_006767.4(LZTR1):c.1333G>A (p.Val445Met) rs201070853 0.00024
NM_006767.4(LZTR1):c.1412G>A (p.Arg471His) rs139031749 0.00021
NM_006767.4(LZTR1):c.2407-18G>A rs542841506 0.00014
NM_006767.4(LZTR1):c.488C>T (p.Thr163Met) rs200806641 0.00014
NM_006767.4(LZTR1):c.372C>T (p.Val124=) rs371891909 0.00006
NM_006767.4(LZTR1):c.1785+19G>A rs777075178 0.00005
NM_006767.4(LZTR1):c.400+10C>T rs375186405 0.00004
NM_006767.4(LZTR1):c.2265G>T (p.Arg755=) rs370009707 0.00002
NM_006767.4(LZTR1):c.2326-6T>C rs199965510 0.00002
NM_006767.4(LZTR1):c.264-9G>T rs377233316 0.00002
NM_006767.4(LZTR1):c.1260+11T>A rs1298556569 0.00001
NM_006767.4(LZTR1):c.2070-8G>T rs768003361 0.00001
NM_006767.4(LZTR1):c.2310G>A (p.Val770=) rs1226268646 0.00001
NM_006767.4(LZTR1):c.1314G>A (p.Glu438=)
NM_006767.4(LZTR1):c.1616-4del
NM_006767.4(LZTR1):c.1700G>A (p.Arg567His) rs372417941
NM_006767.4(LZTR1):c.1785+4T>G rs1924762620
NM_006767.4(LZTR1):c.1901A>C (p.Gln634Pro) rs770312150
NM_006767.4(LZTR1):c.1941T>C (p.Ile647=)
NM_006767.4(LZTR1):c.2070-15G>A rs1601722962
NM_006767.4(LZTR1):c.2326-10G>A rs778909787
NM_006767.4(LZTR1):c.2326-11T>G rs1421950903
NM_006767.4(LZTR1):c.384C>T (p.Ser128=)
NM_006767.4(LZTR1):c.509+6A>G rs1024251271
NM_006767.4(LZTR1):c.628C>A (p.Arg210=) rs150419186
NM_006767.4(LZTR1):c.651+3G>A

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