List of variants in gene NUBPL 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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025152.3(NUBPL):c.*995T>C	rs10136892	0.59892
NM_025152.3(NUBPL):c.*1874A>G	rs10348	0.45711
NM_025152.3(NUBPL):c.*1694G>A	rs1129623	0.44285
NM_025152.3(NUBPL):c.*1685A>G	rs1129622	0.44269
NM_025152.3(NUBPL):c.*312G>A	rs10162516	0.22998
NM_025152.3(NUBPL):c.*1888G>A	rs7148746	0.22286
NM_025152.3(NUBPL):c.*444C>T	rs10162515	0.21109
NM_025152.3(NUBPL):c.*122G>C	rs4981131	0.13131
NM_025152.3(NUBPL):c.*273C>T	rs76188062	0.10021
NM_025152.3(NUBPL):c.*836C>G	rs10147479

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.