List of variants in gene COX10 reported as likely benign for Leigh syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001303.3(COX10):c.-109G>A	rs28680987	0.15186
NM_001303.4(COX10):c.*1267A>G	rs75844637	0.01645
NM_001303.4(COX10):c.*904C>G	rs75839697	0.00276
NM_001303.4(COX10):c.93C>A (p.Asp31Glu)	rs141481210	0.00090
NM_001303.4(COX10):c.302C>T (p.Pro101Leu)	rs145948285	0.00081
NM_001303.4(COX10):c.*1383G>A	rs145948022
NM_001303.4(COX10):c.*646C>G	rs7214082
NM_001303.4(COX10):c.1096G>T (p.Val366Leu)	rs111541535
NM_001303.4(COX10):c.675G>T (p.Pro225=)	rs199609301
NM_001303.4(COX10):c.929-9_929-7dup	rs144296730

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