ClinVar Miner

List of variants in gene NDUFA10 reported as likely pathogenic for Mitochondrial complex 1 deficiency, nuclear type 22

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004544.4(NDUFA10):c.1A>G (p.Met1Val)	rs387906872	0.00001
NM_004544.4(NDUFA10):c.604dup (p.His202fs)	rs746019378

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