ClinVar Miner

List of variants in gene combination LOC130067016, LZTR1 reported as uncertain significance for Hereditary cancer-predisposing syndrome; Cardiovascular phenotype

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.23G>C (p.Gly8Ala) rs764439278 0.00004
NM_006767.4(LZTR1):c.118T>C (p.Tyr40His) rs146436209 0.00001
NM_006767.4(LZTR1):c.47T>C (p.Leu16Pro) rs578100969 0.00001
NM_006767.4(LZTR1):c.55G>C (p.Gly19Arg) rs375788038 0.00001
NM_006767.4(LZTR1):c.59C>T (p.Ala20Val) rs770762358 0.00001
NM_006767.4(LZTR1):c.73G>T (p.Ala25Ser) rs780281625 0.00001
NM_006767.4(LZTR1):c.-3G>A
NM_006767.4(LZTR1):c.-5C>T
NM_006767.4(LZTR1):c.112G>A (p.Val38Ile)
NM_006767.4(LZTR1):c.11C>A (p.Pro4Gln)
NM_006767.4(LZTR1):c.14G>A (p.Gly5Asp)
NM_006767.4(LZTR1):c.17G>A (p.Ser6Asn)
NM_006767.4(LZTR1):c.20C>G (p.Thr7Arg)
NM_006767.4(LZTR1):c.22G>C (p.Gly8Arg) rs575193991
NM_006767.4(LZTR1):c.23G>A (p.Gly8Glu)
NM_006767.4(LZTR1):c.25G>T (p.Gly9Trp)
NM_006767.4(LZTR1):c.25_26delinsTT (p.Gly9Leu)
NM_006767.4(LZTR1):c.26G>A (p.Gly9Glu)
NM_006767.4(LZTR1):c.26G>C (p.Gly9Ala) rs756485244
NM_006767.4(LZTR1):c.26G>T (p.Gly9Val) rs756485244
NM_006767.4(LZTR1):c.35G>A (p.Gly12Glu)
NM_006767.4(LZTR1):c.37G>A (p.Ala13Thr)
NM_006767.4(LZTR1):c.38C>T (p.Ala13Val)
NM_006767.4(LZTR1):c.44C>G (p.Ala15Gly)
NM_006767.4(LZTR1):c.44C>T (p.Ala15Val) rs2147956758
NM_006767.4(LZTR1):c.50C>T (p.Ala17Val)
NM_006767.4(LZTR1):c.52G>T (p.Gly18Cys)
NM_006767.4(LZTR1):c.55G>A (p.Gly19Ser)
NM_006767.4(LZTR1):c.58G>A (p.Ala20Thr) rs1924227635
NM_006767.4(LZTR1):c.5C>G (p.Ala2Gly)
NM_006767.4(LZTR1):c.62G>A (p.Arg21Gln)
NM_006767.4(LZTR1):c.70G>A (p.Val24Ile)
NM_006767.4(LZTR1):c.80G>A (p.Ser27Asn)
NM_006767.4(LZTR1):c.80G>C (p.Ser27Thr) rs776383010

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