ClinVar Miner

List of variants in gene DNM1L reported as pathogenic for cranial nerve neuropathy

Included ClinVar conditions (197):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012062.5(DNM1L):c.1207C>T (p.Arg403Cys) rs863223953
NM_012062.5(DNM1L):c.1292G>A (p.Cys431Tyr) rs1064794656
NM_012062.5(DNM1L):c.575C>A (p.Ala192Glu) rs1555119216
NM_012062.5(DNM1L):c.5A>C (p.Glu2Ala) rs1555229948
NM_012062.5(DNM1L):c.763_764dup (p.Lys256fs) rs1592631789

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.