ClinVar Miner

List of variants in gene COX15, CUTC studied for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 9
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HGVS dbSNP
NM_015960.3(CUTC):c.-68G>A rs886046613
NM_015960.3(CUTC):c.39G>A (p.Ala13=) rs751586131
NM_015960.3(CUTC):c.61+112A>G rs550813748
NM_015960.3(CUTC):c.61+237T>G rs2281636
NM_015960.3(CUTC):c.61+242G>T rs886046616
NM_015960.3(CUTC):c.61+38G>T rs886046615
NM_015960.3(CUTC):c.61+46G>C rs11595470
NM_015960.3(CUTC):c.61+75G>A rs2231675
NM_015960.3(CUTC):c.8G>C (p.Arg3Thr) rs886046614

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