ClinVar Miner

List of variants in gene NUBPL reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_025152.3(NUBPL):c.*1451C>T	rs28533800	0.03631
NM_025152.3(NUBPL):c.*26C>G	rs76130953	0.01425

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