ClinVar Miner

List of variants in gene NDUFAF6 reported as pathogenic for inborn mitochondrial metabolism disorder

Included ClinVar conditions (407):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152416.4(NDUFAF6):c.532G>C (p.Ala178Pro) rs201088736 0.00004
NM_152416.4(NDUFAF6):c.371T>C (p.Ile124Thr) rs201732170 0.00003
NM_152416.4(NDUFAF6):c.420+784C>T rs749738738 0.00002
NM_152416.4(NDUFAF6):c.226T>C (p.Ser76Pro) rs1057519084 0.00001
NM_152416.4(NDUFAF6):c.337C>T (p.Arg113Ter) rs753873681 0.00001
NM_152416.3(NDUFAF6):c.[328G>T];[611C>T]
NM_152416.4(NDUFAF6):c.206A>T (p.Asp69Val) rs1057519085
NM_152416.4(NDUFAF6):c.296A>G (p.Gln99Arg) rs137853184
NM_152416.4(NDUFAF6):c.420+2_420+3insTA rs1829405956
NM_152416.4(NDUFAF6):c.485del (p.Asn162fs) rs762093523
NM_152416.4(NDUFAF6):c.555_559del (p.Tyr187fs) rs1179490149
NM_152416.4(NDUFAF6):c.805C>G (p.His269Asp) rs768273248
NM_152416.4(NDUFAF6):c.820A>G (p.Arg274Gly) rs1057519086

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.