ClinVar Miner

List of variants in gene DNAH11 reported as pathogenic by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_001277115.2(DNAH11):c.12466del (p.Leu4156fs) rs1554292398
NM_001277115.2(DNAH11):c.4333C>T (p.Arg1445Ter) rs72657316
NM_001277115.2(DNAH11):c.6244C>T (p.Arg2082Ter) rs200693106
NM_001277115.2(DNAH11):c.7508_7509insTTG (p.Lys2504_Pro2505insTer) rs797045086
NM_001277115.2(DNAH11):c.8746C>T (p.Gln2916Ter) rs797045085

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.