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: 67
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HGVS dbSNP gnomAD frequency
NM_001369.3(DNAH5):c.3987A>G (p.Lys1329=) rs146191243 0.01011
NM_001369.3(DNAH5):c.5281C>G (p.Arg1761Gly) rs148891849 0.00388
NM_001369.3(DNAH5):c.8757G>C (p.Glu2919Asp) rs115776799 0.00334
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.1356G>A (p.Lys452=) rs144748846 0.00176
NM_001369.3(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270 0.00158
NM_001369.3(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124 0.00139
NM_001369.3(DNAH5):c.3650T>C (p.Ile1217Thr) rs112124692 0.00112
NM_001369.3(DNAH5):c.88C>T (p.Arg30Trp) rs114220185 0.00096
NM_001369.3(DNAH5):c.4373G>A (p.Arg1458Gln) rs61747551 0.00081
NM_001369.3(DNAH5):c.1329G>A (p.Gln443=) rs141621142 0.00076
NM_001369.3(DNAH5):c.8268A>C (p.Ser2756=) rs775185371 0.00046
NM_001369.3(DNAH5):c.8960A>T (p.Asn2987Ile) rs149489069 0.00046
NM_001369.3(DNAH5):c.894C>G (p.Asn298Lys) rs116995413 0.00033
NM_001369.3(DNAH5):c.1752T>C (p.Gly584=) rs201028861 0.00018
NM_001369.3(DNAH5):c.6018T>C (p.Cys2006=) rs368456533 0.00014
NM_001369.3(DNAH5):c.2760A>G (p.Gly920=) rs763731693 0.00013
NM_001369.3(DNAH5):c.13410G>A (p.Ser4470=) rs368920785 0.00010
NM_001369.3(DNAH5):c.2400G>A (p.Glu800=) rs199951976 0.00010
NM_001369.3(DNAH5):c.12123A>C (p.Pro4041=) rs149580135 0.00009
NM_001369.3(DNAH5):c.9619T>C (p.Leu3207=) rs753402995 0.00008
NM_001369.3(DNAH5):c.13155A>T (p.Pro4385=) rs202103048 0.00006
NM_001369.3(DNAH5):c.2235C>T (p.Tyr745=) rs139916610 0.00006
NM_001369.3(DNAH5):c.4071C>T (p.Ser1357=) rs201264488 0.00006
NM_001369.3(DNAH5):c.537G>A (p.Thr179=) rs370805321 0.00006
NM_001369.3(DNAH5):c.7602G>T (p.Ala2534=) rs770309996 0.00006
NM_001369.3(DNAH5):c.2307C>T (p.Ala769=) rs773547505 0.00005
NM_001369.3(DNAH5):c.3086A>T (p.Asp1029Val) rs201338727 0.00004
NM_001369.3(DNAH5):c.5157C>T (p.Phe1719=) rs749688197 0.00004
NM_001369.3(DNAH5):c.6957G>A (p.Thr2319=) rs202042219 0.00004
NM_001369.3(DNAH5):c.888G>A (p.Lys296=) rs758680247 0.00004
NM_001369.3(DNAH5):c.11586G>A (p.Pro3862=) rs755874851 0.00003
NM_001369.3(DNAH5):c.13065G>C (p.Val4355=) rs372488592 0.00003
NM_001369.3(DNAH5):c.4331A>G (p.Asn1444Ser) rs567013299 0.00003
NM_001369.3(DNAH5):c.8925C>T (p.Tyr2975=) rs755490391 0.00003
NM_001369.3(DNAH5):c.12129G>A (p.Thr4043=) rs779527506 0.00002
NM_001369.3(DNAH5):c.13005C>T (p.Thr4335=) rs755271975 0.00002
NM_001369.3(DNAH5):c.1836C>T (p.Tyr612=) rs1035218078 0.00002
NM_001369.3(DNAH5):c.3897T>C (p.Val1299=) rs749416187 0.00002
NM_001369.3(DNAH5):c.5817G>A (p.Ala1939=) rs556936569 0.00002
NM_001369.3(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759 0.00002
NM_001369.3(DNAH5):c.636T>G (p.Gly212=) rs376360357 0.00002
NM_001369.3(DNAH5):c.8772C>T (p.Ala2924=) rs552458966 0.00002
NM_001369.3(DNAH5):c.9918C>T (p.Ile3306=) rs373676166 0.00002
NM_001369.3(DNAH5):c.9975C>T (p.Cys3325=) rs771715883 0.00002
NM_001369.3(DNAH5):c.10909C>T (p.Leu3637=) rs748412220 0.00001
NM_001369.3(DNAH5):c.11463G>A (p.Thr3821=) rs200744540 0.00001
NM_001369.3(DNAH5):c.12861C>T (p.Tyr4287=) rs1389988921 0.00001
NM_001369.3(DNAH5):c.1431C>T (p.His477=) rs1028207982 0.00001
NM_001369.3(DNAH5):c.3747C>T (p.Asp1249=) rs1280894186 0.00001
NM_001369.3(DNAH5):c.4083C>T (p.Pro1361=) rs149691390 0.00001
NM_001369.3(DNAH5):c.5616C>T (p.Asp1872=) rs145129897 0.00001
NM_001369.3(DNAH5):c.8682T>C (p.Pro2894=) rs761409642 0.00001
NM_001369.3(DNAH5):c.910T>C (p.Leu304=) rs754396098 0.00001
NM_001369.3(DNAH5):c.1090-8T>C rs16902950
NM_001369.3(DNAH5):c.11815C>T (p.Leu3939=) rs764968328
NM_001369.3(DNAH5):c.12384C>T (p.Leu4128=) rs772828833
NM_001369.3(DNAH5):c.12765C>T (p.Val4255=) rs561983296
NM_001369.3(DNAH5):c.13095G>A (p.Glu4365=) rs372604448
NM_001369.3(DNAH5):c.13569C>T (p.Asp4523=) rs151080414
NM_001369.3(DNAH5):c.159C>T (p.Thr53=) rs773322142
NM_001369.3(DNAH5):c.1602C>T (p.Asp534=) rs753367747
NM_001369.3(DNAH5):c.1647C>T (p.Asn549=) rs139160176
NM_001369.3(DNAH5):c.5272-9C>T rs555481241
NM_001369.3(DNAH5):c.7335C>T (p.Tyr2445=) rs2127026828
NM_001369.3(DNAH5):c.8316A>G (p.Arg2772=) rs751595453

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