ClinVar Miner

List of variants in gene DNAH5 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 115
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001369.3(DNAH5):c.3834+151G>A rs75164636 0.02410
NM_001369.3(DNAH5):c.1537-50G>A rs150679902 0.01752
NM_001369.3(DNAH5):c.2744-203dup rs145894548 0.01658
NM_001369.3(DNAH5):c.2743+154A>G rs77937662 0.01656
NM_001369.3(DNAH5):c.6989-22T>C rs116215381 0.01633
NM_001369.3(DNAH5):c.3301G>A (p.Val1101Met) rs61747516 0.01505
NM_001369.3(DNAH5):c.10281+65T>C rs76676543 0.01501
NM_001369.3(DNAH5):c.3263-304G>A rs115046790 0.01497
NM_001369.3(DNAH5):c.6688-191A>G rs139556122 0.01484
NM_001369.3(DNAH5):c.3241A>G (p.Met1081Val) rs16902880 0.01472
NM_001369.3(DNAH5):c.11762-283G>T rs62341654 0.01460
NM_001369.3(DNAH5):c.2431+136G>T rs16902905 0.01453
NM_001369.3(DNAH5):c.13126-39G>A rs78940762 0.01324
NM_001369.3(DNAH5):c.5658C>T (p.Tyr1886=) rs6880264 0.01314
NM_001369.3(DNAH5):c.6062-77C>T rs148309622 0.01233
NM_001369.3(DNAH5):c.13338+218G>A rs111321290 0.01220
NM_001369.3(DNAH5):c.976-73T>C rs77141180 0.01219
NM_001369.3(DNAH5):c.1320+132T>C rs77972261 0.01218
NM_001369.3(DNAH5):c.5272-32T>C rs368185722 0.01210
NM_001369.3(DNAH5):c.11028+52G>A rs115374116 0.01208
NM_001369.3(DNAH5):c.660+21C>T rs74611074 0.01194
NM_001369.3(DNAH5):c.3834+74G>A rs114740310 0.01183
NM_001369.3(DNAH5):c.8821-320A>G rs115496041 0.01060
NM_001369.3(DNAH5):c.13338+16C>T rs115271897 0.01021
NM_001369.3(DNAH5):c.2431+71C>T rs77050700 0.01018
NM_001369.3(DNAH5):c.6688-54C>T rs114904056 0.01014
NM_001369.3(DNAH5):c.3987A>G (p.Lys1329=) rs146191243 0.01011
NM_001369.3(DNAH5):c.12909+204G>A rs73749925 0.00992
NM_001369.3(DNAH5):c.4597-64G>A rs115114167 0.00966
NM_001369.3(DNAH5):c.6703T>G (p.Leu2235Val) rs115109673 0.00961
NM_001369.3(DNAH5):c.12499+184G>A rs76029211 0.00942
NM_001369.3(DNAH5):c.6579+20G>A rs115382993 0.00928
NM_001369.3(DNAH5):c.10101+171C>T rs187925010 0.00906
NM_001369.3(DNAH5):c.12909+135G>T rs112104793 0.00875
NM_001369.3(DNAH5):c.1647C>G (p.Asn549Lys) rs139160176 0.00831
NM_001369.3(DNAH5):c.5224T>C (p.Leu1742=) rs35963491 0.00809
NM_001369.3(DNAH5):c.6919G>A (p.Val2307Ile) rs74604638 0.00808
NM_001369.3(DNAH5):c.8647+221T>C rs116352581 0.00808
NM_001369.3(DNAH5):c.6579+6A>G rs141389162 0.00798
NM_001369.3(DNAH5):c.2578-99G>T rs115826876 0.00715
NM_001369.3(DNAH5):c.4596+95A>G rs73746938 0.00593
NM_001369.3(DNAH5):c.7408-205C>T rs192807418 0.00592
NM_001369.3(DNAH5):c.5115-4G>T rs141141086 0.00551
NM_001369.3(DNAH5):c.8821-275G>A rs141301504 0.00538
NM_001369.3(DNAH5):c.2983+291C>T rs140094398 0.00533
NM_001369.3(DNAH5):c.10556-46A>T rs138987164 0.00524
NM_001369.3(DNAH5):c.5115-68G>T rs184097902 0.00462
NM_001369.3(DNAH5):c.*84C>T rs151143347 0.00442
NM_001369.3(DNAH5):c.2743+183C>T rs145627883 0.00438
NM_001369.3(DNAH5):c.2053-23A>C rs114717951 0.00416
NM_001369.3(DNAH5):c.2253C>A (p.Asn751Lys) rs115004914 0.00414
NM_001369.3(DNAH5):c.5281C>G (p.Arg1761Gly) rs148891849 0.00388
NM_001369.3(DNAH5):c.4356-57T>C rs191669243 0.00366
NM_001369.3(DNAH5):c.12465A>G (p.Gln4155=) rs34924315 0.00359
NM_001369.3(DNAH5):c.8757G>C (p.Glu2919Asp) rs115776799 0.00334
NM_001369.3(DNAH5):c.1731-167G>A rs149139577 0.00320
NM_001369.3(DNAH5):c.5266G>A (p.Glu1756Lys) rs116524991 0.00282
NM_001369.3(DNAH5):c.299G>C (p.Gly100Ala) rs144236383 0.00278
NM_001369.3(DNAH5):c.9681A>G (p.Lys3227=) rs138639741 0.00252
NM_001369.3(DNAH5):c.624C>T (p.Asn208=) rs139640247 0.00228
NM_001369.3(DNAH5):c.3514C>A (p.Gln1172Lys) rs141168110 0.00184
NM_001369.3(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270 0.00158
NM_001369.3(DNAH5):c.5882+6G>A rs377640010 0.00158
NM_001369.3(DNAH5):c.8845C>G (p.Gln2949Glu) rs147688221 0.00146
NM_001369.3(DNAH5):c.3262+51T>G rs138034827 0.00130
NM_001369.3(DNAH5):c.13286G>A (p.Arg4429Gln) rs61744047 0.00127
NM_001369.3(DNAH5):c.2443T>A (p.Leu815Met) rs149654950 0.00124
NM_001369.3(DNAH5):c.12472C>T (p.Arg4158Trp) rs3756672 0.00118
NM_001369.3(DNAH5):c.3021G>T (p.Leu1007Phe) rs188638970 0.00103
NM_001369.3(DNAH5):c.342C>T (p.Phe114=) rs145920072 0.00086
NM_001369.3(DNAH5):c.4509C>T (p.Thr1503=) rs138157585 0.00070
NM_001369.3(DNAH5):c.367C>T (p.Leu123Phe) rs148017278 0.00024
NM_001369.3(DNAH5):c.5196G>T (p.Ala1732=) rs201484389 0.00022
NM_001369.3(DNAH5):c.4587G>A (p.Glu1529=) rs569428035 0.00015
NM_001369.3(DNAH5):c.4596+5A>C rs182677317 0.00014
NM_001369.3(DNAH5):c.4440C>T (p.Cys1480=) rs376618204 0.00011
NM_001369.3(DNAH5):c.7888-4A>G rs775268409 0.00008
NM_001369.3(DNAH5):c.6551T>C (p.Val2184Ala) rs200805455 0.00004
NM_001369.3(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759 0.00002
NM_001369.3(DNAH5):c.1090-165_1090-157del rs141723684
NM_001369.3(DNAH5):c.1090-8T>C rs16902950
NM_001369.3(DNAH5):c.11883+66T>A rs150436839
NM_001369.3(DNAH5):c.12033+7A>G rs77541151
NM_001369.3(DNAH5):c.12303C>T (p.Asn4101=) rs2126519296
NM_001369.3(DNAH5):c.1252G>A (p.Ala418Thr)
NM_001369.3(DNAH5):c.13062G>A (p.Ala4354=) rs200924641
NM_001369.3(DNAH5):c.1563G>A (p.Lys521=) rs1580853552
NM_001369.3(DNAH5):c.2053-285A>C rs77992711
NM_001369.3(DNAH5):c.2053-7C>T rs1325993261
NM_001369.3(DNAH5):c.2578-10_2578-7del rs71600031
NM_001369.3(DNAH5):c.2578-13_2578-7dup rs71600031
NM_001369.3(DNAH5):c.2578-15_2578-7dup rs71600031
NM_001369.3(DNAH5):c.2578-7del rs71600031
NM_001369.3(DNAH5):c.2578-9_2578-7del rs71600031
NM_001369.3(DNAH5):c.2931A>C (p.Thr977=) rs1469143674
NM_001369.3(DNAH5):c.3397-174A>G
NM_001369.3(DNAH5):c.3599-57C>T
NM_001369.3(DNAH5):c.3834+194A>G
NM_001369.3(DNAH5):c.3966A>C (p.Ser1322=) rs775449337
NM_001369.3(DNAH5):c.4053+150dup rs3058927
NM_001369.3(DNAH5):c.4117-135C>T
NM_001369.3(DNAH5):c.4597-114_4597-113insATAC rs56036133
NM_001369.3(DNAH5):c.4597-114_4597-113insTATACATATA rs60470226
NM_001369.3(DNAH5):c.5115-289T>C rs114012368
NM_001369.3(DNAH5):c.5272-156_5272-155dup rs147371351
NM_001369.3(DNAH5):c.5272-15dup rs35337694
NM_001369.3(DNAH5):c.5485-220A>T rs2053683
NM_001369.3(DNAH5):c.5712T>C (p.Cys1904=) rs2151857507
NM_001369.3(DNAH5):c.5814G>A (p.Val1938=) rs1580512154
NM_001369.3(DNAH5):c.6989-22del rs753827452
NM_001369.3(DNAH5):c.6989-31dup rs753827452
NM_001369.3(DNAH5):c.7609+77A>G rs147519526
NM_001369.3(DNAH5):c.8010+79_8010+80del
NM_001369.3(DNAH5):c.9721-113_9721-112del rs36092508
NM_001369.3(DNAH5):c.986A>G (p.Glu329Gly)

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.