ClinVar Miner

List of variants in gene NDUFB9 reported as pathogenic for Mitochondrial complex 1 deficiency, nuclear type 24

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_005005.3(NDUFB9):c.431C>T (p.Thr144Met)	rs769883777	0.00014
NM_005005.3(NDUFB9):c.191T>C (p.Leu64Pro)	rs776388520	0.00001

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