ClinVar Miner

List of variants in gene DBT reported as uncertain significance for not provided

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001918.5(DBT):c.1418A>G (p.Asn473Ser) rs75525811 0.00196
NM_001918.5(DBT):c.1127G>A (p.Arg376His) rs150934375 0.00006
NM_001918.5(DBT):c.52-27T>A rs202047153 0.00006
NM_001918.5(DBT):c.1024C>T (p.His342Tyr) rs398123655 0.00001
NM_001918.5(DBT):c.1430T>G (p.Met477Arg) rs398123662 0.00001
NM_001918.5(DBT):c.365A>G (p.Tyr122Cys) rs727503896 0.00001
NM_001918.5(DBT):c.51+5G>C rs398123670 0.00001
NM_001918.5(DBT):c.5C>T (p.Ala2Val) rs398123672 0.00001
NM_001918.5(DBT):c.61C>T (p.Arg21Cys) rs398123673 0.00001
NM_001918.5(DBT):c.1024C>G (p.His342Asp) rs398123655
NM_001918.5(DBT):c.1096T>C (p.Ser366Pro) rs398123656
NM_001918.5(DBT):c.1133A>C (p.Gln378Pro) rs398123657
NM_001918.5(DBT):c.1133A>G (p.Gln378Arg) rs398123657
NM_001918.5(DBT):c.1210-10dup rs398123658
NM_001918.5(DBT):c.1210-11_1210-10inv
NM_001918.5(DBT):c.1258A>G (p.Ile420Val) rs398123659
NM_001918.5(DBT):c.1282-11_1282-5del rs750402853
NM_001918.5(DBT):c.1292G>C (p.Arg431Pro) rs776490043
NM_001918.5(DBT):c.1348G>A (p.Ala450Thr) rs398123661
NM_001918.5(DBT):c.137A>G (p.Lys46Arg) rs794727263
NM_001918.5(DBT):c.209C>T (p.Ser70Leu) rs398123664
NM_001918.5(DBT):c.535C>T (p.Arg179Cys)
NM_001918.5(DBT):c.577G>A (p.Gly193Ser) rs398123671
NM_001918.5(DBT):c.917C>G (p.Ser306Cys) rs794727856

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