ClinVar Miner

List of variants in gene DNAH5 reported as likely benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_001369.2(DNAH5):c.10294G>T (p.Val3432Leu) rs143251588
NM_001369.2(DNAH5):c.10323G>A (p.Met3441Ile) rs149133845
NM_001369.2(DNAH5):c.12346A>G (p.Ile4116Val) rs34920399
NM_001369.2(DNAH5):c.1251C>T (p.Thr417=) rs112911055
NM_001369.2(DNAH5):c.2355C>T (p.Leu785=) rs112238091
NM_001369.2(DNAH5):c.5266G>A (p.Glu1756Lys) rs116524991
NM_001369.2(DNAH5):c.7888-6dupT rs745582136

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.