ClinVar Miner

List of variants in gene COX10 reported as benign for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 10
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NM_001303.3(COX10):c.*1076T>C rs1050216
NM_001303.3(COX10):c.*151_*152delTT rs200239586
NM_001303.3(COX10):c.*322T>C rs11078233
NM_001303.3(COX10):c.*371A>G rs11078234
NM_001303.3(COX10):c.*646C>A rs7214082
NM_001303.3(COX10):c.*757T>C rs1802618
NM_001303.3(COX10):c.*833_*834delCT rs397763766
NM_001303.3(COX10):c.-112G>A rs6502330
NM_001303.3(COX10):c.476G>A (p.Arg159Gln) rs2072279
NM_001303.3(COX10):c.504G>A (p.Leu168=) rs2159132

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