List of variants in gene NDUFA10 reported as benign for Leigh syndrome

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: 29

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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.*3075T>G	rs7588974	0.03737
NM_004544.4(NDUFA10):c.24G>A (p.Leu8=)	rs113012830	0.03541
NM_004544.4(NDUFA10):c.*3349G>A	rs77216981	0.02367
NM_004544.4(NDUFA10):c.*2511C>T	rs74540213	0.01512
NM_004544.4(NDUFA10):c.*396C>G	rs73103629	0.01256
NM_004544.4(NDUFA10):c.*1217A>G	rs116403651	0.01210
NM_004544.4(NDUFA10):c.*2133A>G	rs6736791	0.01130
NM_004544.4(NDUFA10):c.*1878C>T	rs80067639	0.01081
NM_004544.4(NDUFA10):c.*3544C>T	rs114944621	0.01013
NM_004544.4(NDUFA10):c.194A>G (p.Asn65Ser)	rs35715497	0.00925
NM_004544.4(NDUFA10):c.*407C>T	rs74614612	0.00847
NM_004544.4(NDUFA10):c.712G>A (p.Glu238Lys)	rs35462421	0.00570
NM_004544.4(NDUFA10):c.*1382C>T	rs111337344	0.00263
NM_004544.4(NDUFA10):c.*2202C>T	rs77614498	0.00120
NM_004544.4(NDUFA10):c.*2495C>T	rs78395168	0.00119
NM_004544.4(NDUFA10):c.*1229C>G	rs55998047
NM_004544.4(NDUFA10):c.*438C>T	rs13396556

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