ClinVar Miner

List of variants in gene DNAH5 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP
NM_001369.2(DNAH5):c.10784C>T (p.Thr3595Met) rs886043929
NM_001369.2(DNAH5):c.11017T>C (p.Ser3673Pro) rs1250778700
NM_001369.2(DNAH5):c.11018C>T (p.Ser3673Phe) rs1554034235
NM_001369.2(DNAH5):c.11140A>G (p.Ile3714Val) rs143185806
NM_001369.2(DNAH5):c.1121T>C (p.Ile374Thr) rs147499872
NM_001369.2(DNAH5):c.11456-3C>T rs368946226
NM_001369.2(DNAH5):c.11583C>A (p.Ser3861Arg) rs576096758
NM_001369.2(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270
NM_001369.2(DNAH5):c.12655G>A (p.Ala4219Thr) rs794727887
NM_001369.2(DNAH5):c.12842T>C (p.Phe4281Ser) rs886059964
NM_001369.2(DNAH5):c.13070C>G (p.Ala4357Gly) rs368776967
NM_001369.2(DNAH5):c.13753C>A (p.Pro4585Thr)
NM_001369.2(DNAH5):c.13778C>T (p.Thr4593Met) rs142036266
NM_001369.2(DNAH5):c.1585C>T (p.Arg529Trp) rs200452908
NM_001369.2(DNAH5):c.1955G>A (p.Ser652Asn) rs749126116
NM_001369.2(DNAH5):c.2306C>T (p.Ala769Val)
NM_001369.2(DNAH5):c.2431+5G>A rs369244905
NM_001369.2(DNAH5):c.297A>T (p.Gly99=) rs794727633
NM_001369.2(DNAH5):c.3043A>C (p.Thr1015Pro) rs756780275
NM_001369.2(DNAH5):c.3320A>T (p.Tyr1107Phe) rs367913308
NM_001369.2(DNAH5):c.3396G>C (p.Lys1132Asn) rs1554087241
NM_001369.2(DNAH5):c.3734G>A (p.Arg1245His) rs77939839
NM_001369.2(DNAH5):c.3775G>A (p.Ala1259Thr) rs112217391
NM_001369.2(DNAH5):c.3792G>C (p.Arg1264Ser) rs769589158
NM_001369.2(DNAH5):c.4361G>A (p.Arg1454Gln) rs542708170
NM_001369.2(DNAH5):c.4961G>A (p.Arg1654Gln) rs150868941
NM_001369.2(DNAH5):c.5281C>G (p.Arg1761Gly) rs148891849
NM_001369.2(DNAH5):c.5396C>T (p.Ser1799Leu) rs727503903
NM_001369.2(DNAH5):c.5663C>T (p.Thr1888Ile) rs777579934
NM_001369.2(DNAH5):c.574G>A (p.Ala192Thr) rs140700961
NM_001369.2(DNAH5):c.5807C>T (p.Thr1936Ile) rs779609286
NM_001369.2(DNAH5):c.5883-6A>G rs763588282
NM_001369.2(DNAH5):c.5931C>T (p.Ala1977=) rs886043125
NM_001369.2(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759
NM_001369.2(DNAH5):c.661G>A (p.Val221Met) rs1085307485
NM_001369.2(DNAH5):c.6752C>T (p.Thr2251Met) rs146392250
NM_001369.2(DNAH5):c.7444C>T (p.Arg2482Trp) rs1355327016
NM_001369.2(DNAH5):c.7531C>T (p.Arg2511Trp) rs564040169
NM_001369.2(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124
NM_001369.2(DNAH5):c.8002G>A (p.Gly2668Arg) rs147236883
NM_001369.2(DNAH5):c.8030G>A (p.Arg2677Gln) rs886043448
NM_001369.2(DNAH5):c.8731A>G (p.Asn2911Asp) rs142852982
NM_001369.2(DNAH5):c.8845C>G (p.Gln2949Glu) rs147688221
NM_001369.2(DNAH5):c.8925C>T (p.Tyr2975=) rs755490391
NM_001369.2(DNAH5):c.9203A>G (p.Glu3068Gly)
NM_001369.2(DNAH5):c.9229C>T (p.Arg3077Trp) rs1426289211
NM_001369.2(DNAH5):c.9896A>G (p.Gln3299Arg) rs727503902
NM_001369.2(DNAH5):c.9898-6C>T rs1554039568

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.