ClinVar Miner

List of variants in gene DNAH5 reported as likely benign by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_001369.2(DNAH5):c.11463G>A (p.Thr3821=) rs200744540
NM_001369.2(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270
NM_001369.2(DNAH5):c.12123A>C (p.Pro4041=) rs149580135
NM_001369.2(DNAH5):c.13005C>T (p.Thr4335=) rs755271975
NM_001369.2(DNAH5):c.13065G>C (p.Val4355=) rs372488592
NM_001369.2(DNAH5):c.13095G>A (p.Glu4365=) rs372604448
NM_001369.2(DNAH5):c.13155A>T (p.Pro4385=) rs202103048
NM_001369.2(DNAH5):c.1329G>A (p.Gln443=) rs141621142
NM_001369.2(DNAH5):c.13410G>A (p.Ser4470=) rs368920785
NM_001369.2(DNAH5):c.13569C>T (p.Asp4523=) rs151080414
NM_001369.2(DNAH5):c.1431C>T (p.His477=) rs1028207982
NM_001369.2(DNAH5):c.1647C>T (p.Asn549=) rs139160176
NM_001369.2(DNAH5):c.1752T>C (p.Gly584=) rs201028861
NM_001369.2(DNAH5):c.2235C>T (p.Tyr745=) rs139916610
NM_001369.2(DNAH5):c.2307C>T (p.Ala769=) rs773547505
NM_001369.2(DNAH5):c.2400G>A (p.Glu800=) rs199951976
NM_001369.2(DNAH5):c.3514C>A (p.Gln1172Lys) rs141168110
NM_001369.2(DNAH5):c.3650T>C (p.Ile1217Thr) rs112124692
NM_001369.2(DNAH5):c.3897T>C (p.Val1299=) rs749416187
NM_001369.2(DNAH5):c.4071C>T (p.Ser1357=) rs201264488
NM_001369.2(DNAH5):c.4331A>G (p.Asn1444Ser) rs567013299
NM_001369.2(DNAH5):c.5157C>T (p.Phe1719=) rs749688197
NM_001369.2(DNAH5):c.5272-9C>T rs555481241
NM_001369.2(DNAH5):c.5281C>G (p.Arg1761Gly) rs148891849
NM_001369.2(DNAH5):c.537G>A (p.Thr179=) rs370805321
NM_001369.2(DNAH5):c.6018T>C (p.Cys2006=) rs368456533
NM_001369.2(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759
NM_001369.2(DNAH5):c.624C>T (p.Asn208=) rs139640247
NM_001369.2(DNAH5):c.636T>G (p.Gly212=) rs376360357
NM_001369.2(DNAH5):c.7602G>T (p.Ala2534=) rs770309996
NM_001369.2(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124
NM_001369.2(DNAH5):c.8268A>C (p.Ser2756=) rs775185371
NM_001369.2(DNAH5):c.8757G>C (p.Glu2919Asp) rs115776799
NM_001369.2(DNAH5):c.8772C>T (p.Ala2924=) rs552458966
NM_001369.2(DNAH5):c.88C>T (p.Arg30Trp) rs114220185
NM_001369.2(DNAH5):c.894C>G (p.Asn298Lys) rs116995413
NM_001369.2(DNAH5):c.8960A>T (p.Asn2987Ile) rs149489069

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