ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895
NM_001277115.2(DNAH11):c.10780C>T (p.Pro3594Ser) rs746317366
NM_001277115.2(DNAH11):c.12264C>G (p.His4088Gln) rs368428210
NM_001277115.2(DNAH11):c.13167_13177dup (p.Met4393fs) rs1583827297
NM_001277115.2(DNAH11):c.1459C>G (p.Leu487Val) rs759291863
NM_001277115.2(DNAH11):c.180C>T (p.Arg60=) rs781089233
NM_001277115.2(DNAH11):c.3476G>A (p.Arg1159Lys) rs1192624503
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084
NM_001277115.2(DNAH11):c.5528A>C (p.His1843Pro)
NM_001277115.2(DNAH11):c.6352G>A (p.Gly2118Ser) rs72657342
NM_001277115.2(DNAH11):c.6376G>A (p.Val2126Met) rs772530809

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.