ClinVar Miner

List of variants in gene LZTR1 reported as likely pathogenic for Hereditary cancer-predisposing syndrome; Cardiovascular phenotype

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.1396C>T (p.Arg466Trp) rs550922200 0.00006
NM_006767.4(LZTR1):c.1397G>A (p.Arg466Gln) rs587777180 0.00006
NM_006767.4(LZTR1):c.2062C>T (p.Arg688Cys) rs587777178 0.00006
NM_006767.4(LZTR1):c.2387T>C (p.Ile796Thr) rs141672122 0.00005
NM_006767.4(LZTR1):c.1943-1G>A rs1189015572 0.00004
NM_006767.4(LZTR1):c.842C>T (p.Pro281Leu) rs1390048261 0.00003
NM_006767.4(LZTR1):c.1785+1G>A rs145594158 0.00001
NM_006767.4(LZTR1):c.320G>C (p.Arg107Thr) rs1301901369 0.00001
NM_006767.4(LZTR1):c.401-2_401-1del rs769200796 0.00001
NM_006767.4(LZTR1):c.651+1G>T rs1450044732 0.00001
NM_006767.4(LZTR1):c.1149+1G>A rs767191322
NM_006767.4(LZTR1):c.1149+1G>C
NM_006767.4(LZTR1):c.1149+1G>T
NM_006767.4(LZTR1):c.1149G>C (p.Glu383Asp)
NM_006767.4(LZTR1):c.1150-1G>T
NM_006767.4(LZTR1):c.1260+1G>T
NM_006767.4(LZTR1):c.1449+1G>C
NM_006767.4(LZTR1):c.1449+1G>T
NM_006767.4(LZTR1):c.1449G>A (p.Gln483=)
NM_006767.4(LZTR1):c.1449G>C (p.Gln483His)
NM_006767.4(LZTR1):c.1615+1G>A
NM_006767.4(LZTR1):c.1616-1G>A
NM_006767.4(LZTR1):c.1616-1G>C
NM_006767.4(LZTR1):c.1616-2A>C
NM_006767.4(LZTR1):c.1616-2A>G rs1328046881
NM_006767.4(LZTR1):c.1616-2_1616-1delinsCC
NM_006767.4(LZTR1):c.1785+2T>G
NM_006767.4(LZTR1):c.200+1G>T
NM_006767.4(LZTR1):c.200+1dup
NM_006767.4(LZTR1):c.200+2T>A
NM_006767.4(LZTR1):c.200G>C (p.Arg67Pro)
NM_006767.4(LZTR1):c.2069+2T>G
NM_006767.4(LZTR1):c.2070-1G>A
NM_006767.4(LZTR1):c.2070-2A>G rs774954465
NM_006767.4(LZTR1):c.2325+1G>C
NM_006767.4(LZTR1):c.2348_2351del (p.Thr783fs) rs587777179
NM_006767.4(LZTR1):c.264-2A>C
NM_006767.4(LZTR1):c.320+1G>A rs943939913
NM_006767.4(LZTR1):c.320+1G>C rs943939913
NM_006767.4(LZTR1):c.320+2T>G
NM_006767.4(LZTR1):c.321-1G>A
NM_006767.4(LZTR1):c.401-1G>C rs747225246
NM_006767.4(LZTR1):c.401-2del
NM_006767.4(LZTR1):c.509G>T (p.Arg170Leu) rs781431741
NM_006767.4(LZTR1):c.594-1G>C
NM_006767.4(LZTR1):c.594-3C>G
NM_006767.4(LZTR1):c.651+1G>A
NM_006767.4(LZTR1):c.651G>A (p.Glu217=)
NM_006767.4(LZTR1):c.652-1G>A
NM_006767.4(LZTR1):c.652-2A>C
NM_006767.4(LZTR1):c.791+1G>A rs148031742
NM_006767.4(LZTR1):c.791+1G>T
NM_006767.4(LZTR1):c.792-1G>A
NM_006767.4(LZTR1):c.792-2A>G
NM_006767.4(LZTR1):c.993+2T>G
NM_006767.4(LZTR1):c.994-1G>A
NM_006767.4(LZTR1):c.994-1G>T rs758238174
NM_006767.4(LZTR1):c.994-2A>G

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