ClinVar Miner

List of variants in gene DNAH5 reported as uncertain significance by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 160
Download table as spreadsheet
HGVS dbSNP
NM_001369.2(DNAH5):c.10021C>G (p.Leu3341Val) rs751746139
NM_001369.2(DNAH5):c.10036A>G (p.Thr3346Ala) rs141971313
NM_001369.2(DNAH5):c.10044C>T (p.Pro3348=) rs369902800
NM_001369.2(DNAH5):c.10066T>C (p.Leu3356=) rs138441172
NM_001369.2(DNAH5):c.10195G>A (p.Val3399Ile) rs749397968
NM_001369.2(DNAH5):c.10323G>A (p.Met3441Ile) rs149133845
NM_001369.2(DNAH5):c.10347C>T (p.Ala3449=) rs150773884
NM_001369.2(DNAH5):c.10367C>T (p.Ala3456Val) rs149956015
NM_001369.2(DNAH5):c.10646A>G (p.Glu3549Gly) rs758546967
NM_001369.2(DNAH5):c.10658G>A (p.Arg3553Gln)
NM_001369.2(DNAH5):c.11130T>C (p.Arg3710=) rs765391783
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.11376C>T (p.Ala3792=) rs755149967
NM_001369.2(DNAH5):c.11414C>A (p.Thr3805Lys) rs1554027892
NM_001369.2(DNAH5):c.11476C>T (p.Leu3826Phe) rs146750552
NM_001369.2(DNAH5):c.11512G>A (p.Glu3838Lys)
NM_001369.2(DNAH5):c.11974G>C (p.Asp3992His) rs143251480
NM_001369.2(DNAH5):c.12033+7A>C rs77541151
NM_001369.2(DNAH5):c.12076G>A (p.Glu4026Lys) rs776854779
NM_001369.2(DNAH5):c.12105G>A (p.Thr4035=) rs199735129
NM_001369.2(DNAH5):c.12151A>G (p.Met4051Val) rs138162689
NM_001369.2(DNAH5):c.12379C>T (p.Arg4127Cys) rs148696723
NM_001369.2(DNAH5):c.12523G>A (p.Val4175Met) rs148123430
NM_001369.2(DNAH5):c.12558C>T (p.Tyr4186=) rs748817131
NM_001369.2(DNAH5):c.12709G>T (p.Val4237Phe) rs138045391
NM_001369.2(DNAH5):c.12734T>C (p.Met4245Thr) rs766597612
NM_001369.2(DNAH5):c.12880A>G (p.Thr4294Ala) rs765649176
NM_001369.2(DNAH5):c.1290A>G (p.Glu430=) rs990691780
NM_001369.2(DNAH5):c.13077G>A (p.Leu4359=) rs148805204
NM_001369.2(DNAH5):c.13175T>G (p.Phe4392Cys) rs145400611
NM_001369.2(DNAH5):c.13276G>A (p.Glu4426Lys)
NM_001369.2(DNAH5):c.13331G>T (p.Trp4444Leu) rs1060501467
NM_001369.2(DNAH5):c.13569C>A (p.Asp4523Glu) rs151080414
NM_001369.2(DNAH5):c.1362A>G (p.Lys454=) rs371157628
NM_001369.2(DNAH5):c.13672A>G (p.Lys4558Glu) rs752010216
NM_001369.2(DNAH5):c.1475C>T (p.Thr492Met)
NM_001369.2(DNAH5):c.1612G>A (p.Glu538Lys) rs141651575
NM_001369.2(DNAH5):c.1715T>G (p.Leu572Trp) rs137878131
NM_001369.2(DNAH5):c.1810T>C (p.Ser604Pro)
NM_001369.2(DNAH5):c.1884G>A (p.Leu628=) rs534702284
NM_001369.2(DNAH5):c.1904A>G (p.His635Arg)
NM_001369.2(DNAH5):c.1955G>A (p.Ser652Asn) rs749126116
NM_001369.2(DNAH5):c.1982G>A (p.Arg661His) rs185855852
NM_001369.2(DNAH5):c.2259+8A>G rs202137813
NM_001369.2(DNAH5):c.2462A>G (p.Asn821Ser) rs750670743
NM_001369.2(DNAH5):c.2891A>T (p.His964Leu) rs199698421
NM_001369.2(DNAH5):c.3064G>A (p.Val1022Ile) rs375218798
NM_001369.2(DNAH5):c.3154A>C (p.Ser1052Arg)
NM_001369.2(DNAH5):c.3179A>T (p.Lys1060Met) rs145672251
NM_001369.2(DNAH5):c.3302T>C (p.Val1101Ala) rs376453450
NM_001369.2(DNAH5):c.3427C>T (p.Arg1143Cys)
NM_001369.2(DNAH5):c.349G>A (p.Glu117Lys) rs116128702
NM_001369.2(DNAH5):c.360T>C (p.Asp120=) rs368412855
NM_001369.2(DNAH5):c.367C>T (p.Leu123Phe) rs148017278
NM_001369.2(DNAH5):c.3734G>A (p.Arg1245His) rs77939839
NM_001369.2(DNAH5):c.3760C>T (p.Arg1254Trp)
NM_001369.2(DNAH5):c.3775G>A (p.Ala1259Thr) rs112217391
NM_001369.2(DNAH5):c.3777G>A (p.Ala1259=) rs144893234
NM_001369.2(DNAH5):c.378A>G (p.Val126=) rs377275027
NM_001369.2(DNAH5):c.39C>T (p.Ser13=) rs370788337
NM_001369.2(DNAH5):c.4054-4T>C rs200608915
NM_001369.2(DNAH5):c.4082C>G (p.Pro1361Arg)
NM_001369.2(DNAH5):c.4319A>C (p.Glu1440Ala) rs147322363
NM_001369.2(DNAH5):c.4338C>G (p.Leu1446=) rs377432140
NM_001369.2(DNAH5):c.438+5G>C rs776343117
NM_001369.2(DNAH5):c.4480C>T (p.Arg1494Trp) rs535366955
NM_001369.2(DNAH5):c.4525G>A (p.Val1509Met) rs140345677
NM_001369.2(DNAH5):c.4596+5A>C rs182677317
NM_001369.2(DNAH5):c.4689C>T (p.Gly1563=) rs375658702
NM_001369.2(DNAH5):c.4877T>C (p.Met1626Thr) rs753163103
NM_001369.2(DNAH5):c.4961G>A (p.Arg1654Gln) rs150868941
NM_001369.2(DNAH5):c.4995C>T (p.Ile1665=) rs748438142
NM_001369.2(DNAH5):c.5146C>T (p.Arg1716Trp) rs368644722
NM_001369.2(DNAH5):c.5198C>T (p.Ser1733Leu) rs146087064
NM_001369.2(DNAH5):c.5199G>A (p.Ser1733=) rs142806046
NM_001369.2(DNAH5):c.5281C>A (p.Arg1761=) rs148891849
NM_001369.2(DNAH5):c.5392T>C (p.Ser1798Pro) rs1060501468
NM_001369.2(DNAH5):c.5413C>T (p.Arg1805Cys) rs142155986
NM_001369.2(DNAH5):c.5476C>G (p.Pro1826Ala) rs928564123
NM_001369.2(DNAH5):c.5518C>T (p.Arg1840Trp) rs760640325
NM_001369.2(DNAH5):c.553G>A (p.Glu185Lys) rs752339132
NM_001369.2(DNAH5):c.5692G>A (p.Asp1898Asn)
NM_001369.2(DNAH5):c.5714A>G (p.His1905Arg)
NM_001369.2(DNAH5):c.574G>A (p.Ala192Thr) rs140700961
NM_001369.2(DNAH5):c.6381C>T (p.Asn2127=) rs767344710
NM_001369.2(DNAH5):c.660+9G>A rs762915801
NM_001369.2(DNAH5):c.6731A>T (p.Lys2244Met) rs187023993
NM_001369.2(DNAH5):c.6747C>T (p.Phe2249=) rs568499996
NM_001369.2(DNAH5):c.6956C>T (p.Thr2319Met) rs144983881
NM_001369.2(DNAH5):c.6970A>G (p.Thr2324Ala) rs143074036
NM_001369.2(DNAH5):c.7502G>C (p.Arg2501Pro) rs78853309
NM_001369.2(DNAH5):c.7515G>A (p.Glu2505=) rs1032671138
NM_001369.2(DNAH5):c.7525C>T (p.Arg2509Cys) rs531393117
NM_001369.2(DNAH5):c.7531C>T (p.Arg2511Trp) rs564040169
NM_001369.2(DNAH5):c.7684A>T (p.Ile2562Phe) rs151287187
NM_001369.2(DNAH5):c.7752+3A>G rs200385399
NM_001369.2(DNAH5):c.7888-4A>G rs775268409
NM_001369.2(DNAH5):c.7892C>T (p.Thr2631Met) rs375200875
NM_001369.2(DNAH5):c.8002G>A (p.Gly2668Arg) rs147236883
NM_001369.2(DNAH5):c.8190G>A (p.Thr2730=) rs752656841
NM_001369.2(DNAH5):c.8273A>C (p.Glu2758Ala) rs527914224
NM_001369.2(DNAH5):c.8353C>T (p.Pro2785Ser)
NM_001369.2(DNAH5):c.841G>A (p.Val281Ile) rs548585661
NM_001369.2(DNAH5):c.8512A>C (p.Ser2838Arg) rs763198301
NM_001369.2(DNAH5):c.8731A>G (p.Asn2911Asp) rs142852982
NM_001369.2(DNAH5):c.8820+6G>A
NM_001369.2(DNAH5):c.8821-7A>G rs776228125
NM_001369.2(DNAH5):c.8837G>A (p.Arg2946His) rs140975593
NM_001369.2(DNAH5):c.8845C>G (p.Gln2949Glu) rs147688221
NM_001369.2(DNAH5):c.8999G>A (p.Arg3000Gln) rs137949961
NM_001369.2(DNAH5):c.9111T>C (p.Ser3037=) rs765029802
NM_001369.2(DNAH5):c.9125G>A (p.Arg3042Gln) rs200839716
NM_001369.2(DNAH5):c.9203A>G (p.Glu3068Gly) rs141571121
NM_001369.2(DNAH5):c.9213C>T (p.His3071=) rs563907105
NM_001369.2(DNAH5):c.9230G>A (p.Arg3077Gln) rs113742238
NM_001369.2(DNAH5):c.9244C>A (p.Leu3082Ile) rs147372600
NM_001369.2(DNAH5):c.9287G>A (p.Arg3096Gln) rs1388732051
NM_001369.2(DNAH5):c.935T>G (p.Val312Gly) rs762677340
NM_001369.2(DNAH5):c.9461A>C (p.Asp3154Ala) rs149187750
NM_001369.2(DNAH5):c.946C>T (p.Leu316Phe) rs201706790
NM_001369.2(DNAH5):c.9549G>A (p.Gln3183=) rs147865593
NM_001369.2(DNAH5):c.9589C>T (p.Arg3197Trp) rs753913853
NM_001369.2(DNAH5):c.962C>T (p.Ser321Leu) rs201077964
NM_001369.2(DNAH5):c.9677C>T (p.Ala3226Val) rs192262838
NM_001369.2(DNAH5):c.9714C>T (p.Ala3238=) rs375561333
NM_001369.2(DNAH5):c.9720+5G>A rs763440781
NM_001369.2(DNAH5):c.9751G>T (p.Ala3251Ser) rs139293893
NM_001369.2(DNAH5):c.9897+9A>G rs774932799
NM_001369.2(DNAH5):c.9911C>T (p.Ser3304Leu) rs139821753
NM_001369.2(DNAH5):c.9941G>A (p.Arg3314His) rs143858741
NM_001369.3(DNAH5):c.10301A>G (p.Glu3434Gly)
NM_001369.3(DNAH5):c.1165A>G (p.Thr389Ala)
NM_001369.3(DNAH5):c.11803T>C (p.Ser3935Pro)
NM_001369.3(DNAH5):c.12189G>A (p.Gly4063=)
NM_001369.3(DNAH5):c.12248C>A (p.Ala4083Asp)
NM_001369.3(DNAH5):c.12936G>A (p.Glu4312=)
NM_001369.3(DNAH5):c.13513G>T (p.Gly4505Cys)
NM_001369.3(DNAH5):c.13535T>C (p.Val4512Ala)
NM_001369.3(DNAH5):c.13746C>T (p.Tyr4582=)
NM_001369.3(DNAH5):c.13765A>G (p.Lys4589Glu)
NM_001369.3(DNAH5):c.1678G>A (p.Ala560Thr)
NM_001369.3(DNAH5):c.1913A>G (p.Gln638Arg)
NM_001369.3(DNAH5):c.1967C>T (p.Ala656Val)
NM_001369.3(DNAH5):c.2193C>T (p.Val731=)
NM_001369.3(DNAH5):c.259G>A (p.Val87Met)
NM_001369.3(DNAH5):c.3043A>G (p.Thr1015Ala)
NM_001369.3(DNAH5):c.356A>G (p.Asn119Ser)
NM_001369.3(DNAH5):c.4042G>T (p.Asp1348Tyr)
NM_001369.3(DNAH5):c.4355+5G>A
NM_001369.3(DNAH5):c.5563A>G (p.Ile1855Val)
NM_001369.3(DNAH5):c.6498A>G (p.Gly2166=)
NM_001369.3(DNAH5):c.660+10A>G
NM_001369.3(DNAH5):c.6676A>G (p.Ile2226Val)
NM_001369.3(DNAH5):c.7131C>T (p.Phe2377=)
NM_001369.3(DNAH5):c.7445G>A (p.Arg2482Gln)
NM_001369.3(DNAH5):c.7583C>T (p.Ala2528Val)
NM_001369.3(DNAH5):c.882C>T (p.Leu294=)
NM_001369.3(DNAH5):c.912G>A (p.Leu304=)
NM_001369.3(DNAH5):c.9871T>C (p.Leu3291=)

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.