ClinVar Miner

List of variants studied for Mitochondrial complex 1 deficiency, nuclear type 4 by Baylor Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_007103.4(NDUFV1):c.1157G>A (p.Arg386His) rs536758576 0.00009
NM_007103.4(NDUFV1):c.1022C>T (p.Ala341Val) rs121913660 0.00006
NM_007103.4(NDUFV1):c.166T>C (p.Ser56Pro) rs201727685 0.00005
NM_007103.4(NDUFV1):c.312G>T (p.Lys104Asn) rs768399541 0.00002
NM_007103.4(NDUFV1):c.499T>G (p.Ser167Ala) rs773368756
NM_007103.4(NDUFV1):c.853C>A (p.Pro285Thr)
NM_007103.4(NDUFV1):c.961G>A (p.Gly321Ser)
NM_007103.4(NDUFV1):c.995_1000del (p.Cys332_Thr334delinsSer)

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.