ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP
NM_001277115.2(DNAH11):c.100G>T (p.Glu34Ter) rs2285943
NM_001277115.2(DNAH11):c.100_101delinsTT (p.Glu34Leu) rs398123604
NM_001277115.2(DNAH11):c.101A>T (p.Glu34Val) rs2285944
NM_001277115.2(DNAH11):c.10399G>A (p.Ala3467Thr) rs2214326
NM_001277115.2(DNAH11):c.10739G>A (p.Arg3580His) rs34879202
NM_001277115.2(DNAH11):c.10976C>T (p.Ala3659Val) rs150631721
NM_001277115.2(DNAH11):c.11402C>G (p.Pro3801Arg) rs146362213
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln) rs113653972
NM_001277115.2(DNAH11):c.1426-9T>C rs72655983
NM_001277115.2(DNAH11):c.2454A>G (p.Ala818=) rs4615458
NM_001277115.2(DNAH11):c.2835A>G (p.Gln945=) rs17144747
NM_001277115.2(DNAH11):c.4377+15A>G rs57208694
NM_001277115.2(DNAH11):c.4378-17_4378-16insATTTA rs57952953
NM_001277115.2(DNAH11):c.4430T>C (p.Val1477Ala) rs72657320
NM_001277115.2(DNAH11):c.4449T>C (p.Ile1483=) rs56029521
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=) rs55666134
NM_001277115.2(DNAH11):c.5621+11A>T rs59447021
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met) rs72655972
NM_001277115.2(DNAH11):c.640A>G (p.Ile214Val) rs117064287
NM_001277115.2(DNAH11):c.705C>T (p.Asn235=) rs10950854
NM_001277115.2(DNAH11):c.7290C>T (p.Phe2430=) rs12536928
NM_001277115.2(DNAH11):c.8266T>C (p.Cys2756Arg) rs74667361
NM_001277115.2(DNAH11):c.8362C>G (p.His2788Asp) rs147478795
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) rs201207627

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.