ClinVar Miner

List of variants in gene DNAH5 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
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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.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.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.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.2743+183C>T rs145627883 0.00438
NM_001369.3(DNAH5):c.2053-23A>C rs114717951 0.00416
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.1731-167G>A rs149139577 0.00320
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.3262+51T>G rs138034827 0.00130
NM_001369.3(DNAH5):c.13286G>A (p.Arg4429Gln) rs61744047 0.00127
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.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.2053-285A>C rs77992711
NM_001369.3(DNAH5):c.2577+5T>G rs201596289
NM_001369.3(DNAH5):c.2578-10_2578-7del rs71600031
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.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.5485-220A>T rs2053683
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

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