ClinVar Miner

List of variants studied for Leigh syndrome; Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency by Fulgent Genetics,Fulgent Genetics

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Total variants: 3
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NM_001303.4(COX10):c.1027T>C (p.Cys343Arg) rs200818252
NM_001303.4(COX10):c.1061G>A (p.Arg354Gln) rs745492359
NM_001303.4(COX10):c.311C>T (p.Pro104Leu) rs202207627

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