ClinVar Miner

List of variants in gene LOC130067016, LZTR1 studied for Hereditary cancer-predisposing syndrome; Cardiovascular phenotype

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Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.-4C>T rs573275770 0.00019
NM_006767.4(LZTR1):c.54C>G (p.Gly18=) rs371007598 0.00015
NM_006767.4(LZTR1):c.96T>C (p.His32=) rs372440263 0.00015
NM_006767.4(LZTR1):c.21G>A (p.Thr7=) rs377622689 0.00006
NM_006767.4(LZTR1):c.23G>C (p.Gly8Ala) rs764439278 0.00004
NM_006767.4(LZTR1):c.27G>A (p.Gly9=) rs750714248 0.00003
NM_006767.4(LZTR1):c.115G>T (p.Glu39Ter) rs762434811 0.00001
NM_006767.4(LZTR1):c.118T>C (p.Tyr40His) rs146436209 0.00001
NM_006767.4(LZTR1):c.36G>A (p.Gly12=) rs756364667 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.-2G>A
NM_006767.4(LZTR1):c.-3G>A
NM_006767.4(LZTR1):c.-5C>T
NM_006767.4(LZTR1):c.102C>T (p.Cys34=)
NM_006767.4(LZTR1):c.104C>T (p.Ser35Leu)
NM_006767.4(LZTR1):c.108C>T (p.Asp36=)
NM_006767.4(LZTR1):c.112G>A (p.Val38Ile)
NM_006767.4(LZTR1):c.114C>T (p.Val38=)
NM_006767.4(LZTR1):c.11C>A (p.Pro4Gln)
NM_006767.4(LZTR1):c.11C>T (p.Pro4Leu)
NM_006767.4(LZTR1):c.120C>G (p.Tyr40Ter)
NM_006767.4(LZTR1):c.123G>C (p.Leu41=)
NM_006767.4(LZTR1):c.12G>A (p.Pro4=)
NM_006767.4(LZTR1):c.14G>A (p.Gly5Asp)
NM_006767.4(LZTR1):c.16A>C (p.Ser6Arg)
NM_006767.4(LZTR1):c.17G>A (p.Ser6Asn)
NM_006767.4(LZTR1):c.19_21delinsCC (p.Thr7fs)
NM_006767.4(LZTR1):c.19del (p.Thr7fs)
NM_006767.4(LZTR1):c.1A>G (p.Met1Val) rs1569152752
NM_006767.4(LZTR1):c.20C>G (p.Thr7Arg)
NM_006767.4(LZTR1):c.20del (p.Thr7fs)
NM_006767.4(LZTR1):c.21G>C (p.Thr7=)
NM_006767.4(LZTR1):c.21G>T (p.Thr7=)
NM_006767.4(LZTR1):c.22G>A (p.Gly8Arg)
NM_006767.4(LZTR1):c.22G>C (p.Gly8Arg) rs575193991
NM_006767.4(LZTR1):c.22G>T (p.Gly8Trp) rs575193991
NM_006767.4(LZTR1):c.23G>A (p.Gly8Glu)
NM_006767.4(LZTR1):c.23G>T (p.Gly8Val)
NM_006767.4(LZTR1):c.24G>C (p.Gly8=)
NM_006767.4(LZTR1):c.25G>T (p.Gly9Trp)
NM_006767.4(LZTR1):c.25_26delinsA (p.Gly9fs)
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.27del (p.Gln10fs) rs587777613
NM_006767.4(LZTR1):c.27dup (p.Gln10fs) rs587777613
NM_006767.4(LZTR1):c.29A>C (p.Gln10Pro)
NM_006767.4(LZTR1):c.33C>T (p.Ile11=)
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.3G>A (p.Met1Ile)
NM_006767.4(LZTR1):c.42G>A (p.Ala14=) rs1446469999
NM_006767.4(LZTR1):c.42G>C (p.Ala14=) rs1446469999
NM_006767.4(LZTR1):c.42_44delinsCG (p.Leu16fs)
NM_006767.4(LZTR1):c.44C>G (p.Ala15Gly)
NM_006767.4(LZTR1):c.44C>T (p.Ala15Val) rs2147956758
NM_006767.4(LZTR1):c.45C>T (p.Ala15=)
NM_006767.4(LZTR1):c.46C>G (p.Leu16Val)
NM_006767.4(LZTR1):c.47T>G (p.Leu16Arg)
NM_006767.4(LZTR1):c.48G>A (p.Leu16=)
NM_006767.4(LZTR1):c.48G>C (p.Leu16=)
NM_006767.4(LZTR1):c.48G>T (p.Leu16=)
NM_006767.4(LZTR1):c.50C>T (p.Ala17Val)
NM_006767.4(LZTR1):c.50_51del (p.Ala17fs)
NM_006767.4(LZTR1):c.52G>T (p.Gly18Cys)
NM_006767.4(LZTR1):c.53G>A (p.Gly18Asp)
NM_006767.4(LZTR1):c.54C>A (p.Gly18=)
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.5_11dup (p.Gly5fs)
NM_006767.4(LZTR1):c.60G>T (p.Ala20=)
NM_006767.4(LZTR1):c.62G>A (p.Arg21Gln)
NM_006767.4(LZTR1):c.62G>C (p.Arg21Pro) rs1469540056
NM_006767.4(LZTR1):c.63G>T (p.Arg21=)
NM_006767.4(LZTR1):c.65C>T (p.Ser22Phe)
NM_006767.4(LZTR1):c.70G>A (p.Val24Ile)
NM_006767.4(LZTR1):c.75C>T (p.Ala25=) rs1924228731
NM_006767.4(LZTR1):c.77del (p.Pro26fs)
NM_006767.4(LZTR1):c.80G>A (p.Ser27Asn)
NM_006767.4(LZTR1):c.80G>C (p.Ser27Thr) rs776383010
NM_006767.4(LZTR1):c.80G>T (p.Ser27Ile)
NM_006767.4(LZTR1):c.87C>T (p.Asp29=)
NM_006767.4(LZTR1):c.94C>T (p.His32Tyr)
NM_006767.4(LZTR1):c.96T>A (p.His32Gln)

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