List of variants in gene NDUFA10 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004544.4(NDUFA10):c.1923_1924insA	rs138899326	0.11754
NM_004544.4(NDUFA10):c.*647C>T	rs116254382	0.00794
NM_004544.4(NDUFA10):c.*1453G>A	rs192964209	0.00706
NM_004544.4(NDUFA10):c.712G>A (p.Glu238Lys)	rs35462421	0.00570
NM_004544.4(NDUFA10):c.-38T>G	rs374970309	0.00206
NM_004544.4(NDUFA10):c.*679A>G	rs374065697	0.00027
NM_004544.4(NDUFA10):c.*183C>T	rs112660586	0.00023
NM_004544.4(NDUFA10):c.404T>C (p.Leu135Ser)	rs140776586	0.00020
NM_004544.4(NDUFA10):c.*428C>T	rs557106858	0.00004
NM_004544.4(NDUFA10):c.*1930C>G	rs535714073	0.00001
NM_004544.4(NDUFA10):c.1000-5del	rs138479490

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