ClinVar Miner

List of variants in gene DNAH5 reported as benign for Ciliary dyskinesia, primary, 3

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Gene type:
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Total variants: 86
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HGVS dbSNP
NM_001369.2(DNAH5):c.*1048A>G rs2896111
NM_001369.2(DNAH5):c.*1591T>A
NM_001369.2(DNAH5):c.*649G>C rs77289648
NM_001369.2(DNAH5):c.*775G>A
NM_001369.2(DNAH5):c.10102-29C>T rs6554813
NM_001369.2(DNAH5):c.10140A>G (p.Glu3380=) rs6554812
NM_001369.2(DNAH5):c.10457T>C (p.Met3486Thr) rs141651941
NM_001369.2(DNAH5):c.10473G>A (p.Thr3491=) rs2401809
NM_001369.2(DNAH5):c.1090-8T>C rs16902950
NM_001369.2(DNAH5):c.11570+35A>G rs3734109
NM_001369.2(DNAH5):c.11762-45T>C rs3777093
NM_001369.2(DNAH5):c.1198-24C>A rs13180591
NM_001369.2(DNAH5):c.1198-45A>G rs13162553
NM_001369.2(DNAH5):c.12033+7A>G rs77541151
NM_001369.2(DNAH5):c.12034-24T>C rs17203442
NM_001369.2(DNAH5):c.12401C>T (p.Ala4134Val) rs30168
NM_001369.2(DNAH5):c.12468A>C (p.Gly4156=) rs30169
NM_001369.2(DNAH5):c.12658A>G (p.Thr4220Ala) rs2277046
NM_001369.2(DNAH5):c.12708T>C (p.Gly4236=) rs61744054
NM_001369.2(DNAH5):c.12910-11C>T rs30175
NM_001369.2(DNAH5):c.13071C>T (p.Ala4357=) rs10077457
NM_001369.2(DNAH5):c.13348A>G (p.Ile4450Val) rs3734110
NM_001369.2(DNAH5):c.13359A>G (p.Thr4453=) rs3734111
NM_001369.2(DNAH5):c.13462C>A (p.Pro4488Thr) rs113425437
NM_001369.2(DNAH5):c.13491+37A>G rs10069041
NM_001369.2(DNAH5):c.13724-35T>A rs2166337
NM_001369.2(DNAH5):c.1395C>T (p.Ser465=) rs34580014
NM_001369.2(DNAH5):c.1503T>C (p.Ile501=) rs3213936
NM_001369.2(DNAH5):c.1647C>G (p.Asn549Lys) rs139160176
NM_001369.2(DNAH5):c.1672A>G (p.Thr558Ala) rs1530498
NM_001369.2(DNAH5):c.1772T>G (p.Leu591Arg) rs35090077
NM_001369.2(DNAH5):c.192+14C>G rs1530497
NM_001369.2(DNAH5):c.2053-23A>C rs114717951
NM_001369.2(DNAH5):c.2229T>C (p.Asp743=) rs1445823
NM_001369.2(DNAH5):c.2253C>A (p.Asn751Lys) rs115004914
NM_001369.2(DNAH5):c.2296A>T (p.Ile766Leu) rs4701997
NM_001369.2(DNAH5):c.2683G>A (p.Glu895Lys) rs76229167
NM_001369.2(DNAH5):c.3175-34G>A rs13170062
NM_001369.2(DNAH5):c.3258T>C (p.Leu1086=) rs10057007
NM_001369.2(DNAH5):c.3301G>A (p.Val1101Met) rs61747516
NM_001369.2(DNAH5):c.36T>G (p.His12Gln) rs339445
NM_001369.2(DNAH5):c.3834+40C>T rs35621834
NM_001369.2(DNAH5):c.4053+32C>T rs13156044
NM_001369.2(DNAH5):c.4152A>G (p.Thr1384=) rs7703349
NM_001369.2(DNAH5):c.4374G>T (p.Arg1458=) rs6554827
NM_001369.2(DNAH5):c.4431C>T (p.Ser1477=) rs74451896
NM_001369.2(DNAH5):c.4796+41G>A rs7704417
NM_001369.2(DNAH5):c.4797-29C>A rs1502043
NM_001369.2(DNAH5):c.5114+11T>C rs6554820
NM_001369.2(DNAH5):c.5114+22A>T rs4701988
NM_001369.2(DNAH5):c.5115-49G>C rs10041099
NM_001369.2(DNAH5):c.5115-5T>C rs4429853
NM_001369.2(DNAH5):c.5172C>T (p.Ala1724=) rs10041113
NM_001369.2(DNAH5):c.5272-39T>A rs1910089
NM_001369.2(DNAH5):c.5658C>T (p.Tyr1886=) rs6880264
NM_001369.2(DNAH5):c.58-13T>C rs115758625
NM_001369.2(DNAH5):c.6264C>T (p.Ala2088=) rs1348689
NM_001369.2(DNAH5):c.6444+11C>T rs1348691
NM_001369.2(DNAH5):c.6444+8A>G rs1348690
NM_001369.2(DNAH5):c.6989-13T>C rs112344370
NM_001369.2(DNAH5):c.71G>A (p.Gly24Glu) rs1530496
NM_001369.2(DNAH5):c.7230+32A>G rs56046501
NM_001369.2(DNAH5):c.7274G>A (p.Arg2425His) rs35900306
NM_001369.2(DNAH5):c.7388A>G (p.Gln2463Arg) rs10078391
NM_001369.2(DNAH5):c.7609+19C>T rs35732567
NM_001369.2(DNAH5):c.8449-12T>C rs111313933
NM_001369.2(DNAH5):c.8586G>T (p.Leu2862Phe) rs10513155
NM_001369.2(DNAH5):c.9522G>A (p.Thr3174=) rs35233147
NM_001369.2(DNAH5):c.9721-12A>T rs12655133
NM_001369.2(DNAH5):c.975+30A>C rs35925547
NM_001369.3(DNAH5):c.11761+93G>T
NM_001369.3(DNAH5):c.1198-68C>T
NM_001369.3(DNAH5):c.1320+269T>A
NM_001369.3(DNAH5):c.1320+73T>C
NM_001369.3(DNAH5):c.13491+66T>C
NM_001369.3(DNAH5):c.277+118A>G
NM_001369.3(DNAH5):c.3397-51T>C
NM_001369.3(DNAH5):c.4053+64G>A
NM_001369.3(DNAH5):c.4054-59T>C
NM_001369.3(DNAH5):c.4796+264A>C
NM_001369.3(DNAH5):c.4796+57A>C
NM_001369.3(DNAH5):c.4797-93C>A
NM_001369.3(DNAH5):c.5710-58G>A
NM_001369.3(DNAH5):c.6687+110A>G
NM_001369.3(DNAH5):c.6842-78C>T
NM_001369.3(DNAH5):c.799-11C>T

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