ClinVar Miner

List of variants in gene OTC studied for Inborn genetic diseases

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000531.6(OTC):c.137A>G (p.Lys46Arg) rs1800321 0.26575
NM_000531.6(OTC):c.299-8T>A rs73196229 0.15031
NM_000531.6(OTC):c.809A>G (p.Gln270Arg) rs1800328 0.02868
NM_000531.6(OTC):c.751T>C (p.Leu251=) rs36005267 0.00722
NM_000531.6(OTC):c.429T>C (p.Tyr143=) rs145777402 0.00341
NM_000531.6(OTC):c.298+5G>C rs72554348 0.00058
NM_000531.6(OTC):c.941A>C (p.Glu314Ala) rs137899554 0.00028
NM_000531.6(OTC):c.621C>T (p.Ser207=) rs72558415 0.00005
NM_000531.6(OTC):c.85C>G (p.Gln29Glu) rs752916728 0.00004
NM_000531.6(OTC):c.270T>C (p.Ser90=) rs72554342 0.00003
NM_000531.6(OTC):c.272C>T (p.Thr91Ile) rs372906667 0.00002
NM_000531.6(OTC):c.89C>A (p.Pro30Gln) rs753712951 0.00002
NM_000531.6(OTC):c.717+5G>A rs747637190 0.00001
NM_000531.6(OTC):c.179C>G (p.Ser60Ter)
NM_000531.6(OTC):c.210A>G (p.Lys70=)
NM_000531.6(OTC):c.656C>A (p.Thr219Asn)
NM_000531.6(OTC):c.682A>T (p.Ser228Cys)
NM_000531.6(OTC):c.77G>A (p.Arg26Gln) rs68031618
NM_000531.6(OTC):c.953CTC[1] (p.Pro319del) rs1555976710
NM_000531.6(OTC):c.958C>T (p.Arg320Ter) rs72558473

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