ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by EGL Genetic Diagnostics, Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
Download table as spreadsheet
HGVS dbSNP
NM_001277115.2(DNAH11):c.10041T>A (p.Asn3347Lys) rs772016314
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895
NM_001277115.2(DNAH11):c.10631A>G (p.Glu3544Gly) rs928335497
NM_001277115.2(DNAH11):c.11691-19delinsTG rs373641344
NM_001277115.2(DNAH11):c.11691-20dup rs5882827
NM_001277115.2(DNAH11):c.11717C>G (p.Ala3906Gly) rs200664169
NM_001277115.2(DNAH11):c.1220A>C (p.Asp407Ala) rs780042783
NM_001277115.2(DNAH11):c.12509C>G (p.Thr4170Ser) rs12537531
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703
NM_001277115.2(DNAH11):c.1671A>C (p.Glu557Asp) rs764968620
NM_001277115.2(DNAH11):c.1720A>G (p.Ile574Val) rs374359812
NM_001277115.2(DNAH11):c.2038G>A (p.Asp680Asn) rs201121146
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255
NM_001277115.2(DNAH11):c.2486G>A (p.Arg829His) rs201261243
NM_001277115.2(DNAH11):c.2631C>A (p.Ile877=) rs1003575600
NM_001277115.2(DNAH11):c.2682C>T (p.Leu894=) rs149926178
NM_001277115.2(DNAH11):c.3466G>A (p.Gly1156Arg) rs183521702
NM_001277115.2(DNAH11):c.3853-5C>G rs367628980
NM_001277115.2(DNAH11):c.4001T>C (p.Ile1334Thr) rs72657309
NM_001277115.2(DNAH11):c.4294T>G (p.Leu1432Val) rs794727390
NM_001277115.2(DNAH11):c.5501G>A (p.Arg1834His) rs750430725
NM_001277115.2(DNAH11):c.5622-7C>A rs727503901
NM_001277115.2(DNAH11):c.571C>T (p.His191Tyr) rs562163349
NM_001277115.2(DNAH11):c.5936T>C (p.Leu1979Pro) rs772070316
NM_001277115.2(DNAH11):c.7039A>G (p.Thr2347Ala) rs794727671
NM_001277115.2(DNAH11):c.7325A>G (p.Lys2442Arg) rs114286628
NM_001277115.2(DNAH11):c.9499A>C (p.Thr3167Pro) rs202224167
NM_001277115.2(DNAH11):c.9572C>T (p.Thr3191Ile) rs760597183
NM_001277115.2(DNAH11):c.9640G>A (p.Ala3214Thr) rs141979671

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.