List of variants in gene NDUFA10 reported as benign for Mitochondrial complex I deficiency, nuclear type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_004544.4(NDUFA10):c.105A>G (p.Lys35=)	rs2083411	0.70392
NM_004544.4(NDUFA10):c.*3450G>A	rs7573892	0.59554
NM_004544.4(NDUFA10):c.*1957G>A	rs4854069	0.55325
NM_004544.4(NDUFA10):c.771A>G (p.Gln257=)	rs13848	0.38961
NM_004544.4(NDUFA10):c.*1189C>T	rs66534347	0.30437
NM_004544.4(NDUFA10):c.*414G>A	rs13424612	0.28510
NM_004544.4(NDUFA10):c.*3204C>T	rs34277046	0.28460
NM_004544.4(NDUFA10):c.5C>G (p.Ala2Gly)	rs11541494	0.11689
NM_004544.4(NDUFA10):c.*308C>T	rs8369	0.11658
NM_004544.4(NDUFA10):c.*2309G>A	rs1132778	0.11433
NM_004544.4(NDUFA10):c.*2602C>T	rs58261980	0.10946
NM_004544.4(NDUFA10):c.*631C>T	rs10933622	0.05326
NM_004544.4(NDUFA10):c.24G>A (p.Leu8=)	rs113012830	0.03541
NM_004544.4(NDUFA10):c.*396C>G	rs73103629	0.01256
NM_004544.4(NDUFA10):c.*1229C>G	rs55998047
NM_004544.4(NDUFA10):c.*438C>T	rs13396556

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