ClinVar Miner

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

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_000531.6(OTC):c.-106C>A rs749748052
NM_000531.6(OTC):c.-4G>A rs796052014
NM_000531.6(OTC):c.1019C>T (p.Ser340Phe) rs1569282905
NM_000531.6(OTC):c.122A>T (p.Asp41Val) rs74518351
NM_000531.6(OTC):c.354G>A (p.Leu118=) rs1057518540
NM_000531.6(OTC):c.374C>T (p.Thr125Met) rs72554356
NM_000531.6(OTC):c.382G>C (p.Ala128Pro) rs886043507
NM_000531.6(OTC):c.433C>A (p.Gln145Lys) rs753584565
NM_000531.6(OTC):c.470T>C (p.Ile157Thr) rs1569279421
NM_000531.6(OTC):c.520G>A (p.Ala174Thr) rs72556281
NM_000531.6(OTC):c.572T>G (p.Leu191Arg) rs72556297
NM_000531.6(OTC):c.608C>T (p.Ser203Phe) rs72558410
NM_000531.6(OTC):c.626C>G (p.Ala209Gly) rs72558417
NM_000531.6(OTC):c.725C>A (p.Thr242Asn) rs72558435
NM_000531.6(OTC):c.76C>T (p.Arg26Trp) rs1057515879
NM_000531.6(OTC):c.808C>G (p.Gln270Glu) rs72558451
NM_000531.6(OTC):c.868-3T>C rs398123459
NM_000531.6(OTC):c.870T>C (p.Thr290=) rs794727959

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