ClinVar Miner

List of variants in gene DNAH5 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 107
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HGVS dbSNP
NM_001369.2(DNAH5):c.10140A>G (p.Glu3380=) rs6554812
NM_001369.2(DNAH5):c.10195G>A (p.Val3399Ile) rs749397968
NM_001369.2(DNAH5):c.10294G>T (p.Val3432Leu) rs143251588
NM_001369.2(DNAH5):c.10323G>A (p.Met3441Ile) rs149133845
NM_001369.2(DNAH5):c.10457T>C (p.Met3486Thr) rs141651941
NM_001369.2(DNAH5):c.10473G>A (p.Thr3491=) rs2401809
NM_001369.2(DNAH5):c.10545A>G (p.Lys3515=) rs727502972
NM_001369.2(DNAH5):c.11437C>T (p.Arg3813Trp) rs140948493
NM_001369.2(DNAH5):c.11570+8T>C rs369789559
NM_001369.2(DNAH5):c.11869G>A (p.Asp3957Asn) rs749548708
NM_001369.2(DNAH5):c.11974G>C (p.Asp3992His) rs143251480
NM_001369.2(DNAH5):c.12033+7A>G rs77541151
NM_001369.2(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270
NM_001369.2(DNAH5):c.12209C>T (p.Thr4070Ile) rs746662023
NM_001369.2(DNAH5):c.12401C>T (p.Ala4134Val) rs30168
NM_001369.2(DNAH5):c.12468A>C (p.Gly4156=) rs30169
NM_001369.2(DNAH5):c.12658A>G (p.Thr4220Ala) rs2277046
NM_001369.2(DNAH5):c.12708T>C (p.Gly4236=) rs61744054
NM_001369.2(DNAH5):c.12910-11C>T rs30175
NM_001369.2(DNAH5):c.13071C>T (p.Ala4357=) rs10077457
NM_001369.2(DNAH5):c.13194_13197del (p.Asp4398fs) rs727502971
NM_001369.2(DNAH5):c.1321-15T>C rs202081804
NM_001369.2(DNAH5):c.13348A>G (p.Ile4450Val) rs3734110
NM_001369.2(DNAH5):c.13359A>G (p.Thr4453=) rs3734111
NM_001369.2(DNAH5):c.13462C>A (p.Pro4488Thr) rs113425437
NM_001369.2(DNAH5):c.13492-15T>C rs192514899
NM_001369.2(DNAH5):c.13569C>A (p.Asp4523Glu) rs151080414
NM_001369.2(DNAH5):c.1356G>A (p.Lys452=) rs144748846
NM_001369.2(DNAH5):c.1395C>T (p.Ser465=) rs34580014
NM_001369.2(DNAH5):c.1427_1428del (p.Phe476fs) rs774493427
NM_001369.2(DNAH5):c.1503T>C (p.Ile501=) rs3213936
NM_001369.2(DNAH5):c.1647C>G (p.Asn549Lys) rs139160176
NM_001369.2(DNAH5):c.1672A>G (p.Thr558Ala) rs1530498
NM_001369.2(DNAH5):c.1715T>G (p.Leu572Trp) rs137878131
NM_001369.2(DNAH5):c.1772T>G (p.Leu591Arg) rs35090077
NM_001369.2(DNAH5):c.1858C>A (p.Gln620Lys) rs34076967
NM_001369.2(DNAH5):c.192+14C>G rs1530497
NM_001369.2(DNAH5):c.2229T>C (p.Asp743=) rs1445823
NM_001369.2(DNAH5):c.2253C>A (p.Asn751Lys) rs115004914
NM_001369.2(DNAH5):c.2296A>T (p.Ile766Leu) rs4701997
NM_001369.2(DNAH5):c.2578-10_2578-7del rs71600031
NM_001369.2(DNAH5):c.2578-8_2578-7del rs71600031
NM_001369.2(DNAH5):c.2578-9_2578-7del rs71600031
NM_001369.2(DNAH5):c.2683G>A (p.Glu895Lys) rs76229167
NM_001369.2(DNAH5):c.3016A>G (p.Ser1006Gly) rs16902886
NM_001369.2(DNAH5):c.3037_3040del (p.Val1014fs) rs1580731750
NM_001369.2(DNAH5):c.3241A>G (p.Met1081Val) rs16902880
NM_001369.2(DNAH5):c.3258T>C (p.Leu1086=) rs10057007
NM_001369.2(DNAH5):c.3301G>A (p.Val1101Met) rs61747516
NM_001369.2(DNAH5):c.3514C>A (p.Gln1172Lys) rs141168110
NM_001369.2(DNAH5):c.3534C>T (p.Asn1178=) rs151274810
NM_001369.2(DNAH5):c.36T>G (p.His12Gln) rs339445
NM_001369.2(DNAH5):c.3835-3del rs35398031
NM_001369.2(DNAH5):c.3895G>T (p.Val1299Phe) rs767853104
NM_001369.2(DNAH5):c.3987A>G (p.Lys1329=) rs146191243
NM_001369.2(DNAH5):c.4152A>G (p.Thr1384=) rs7703349
NM_001369.2(DNAH5):c.4374G>T (p.Arg1458=) rs6554827
NM_001369.2(DNAH5):c.4510G>C (p.Gly1504Arg) rs143567667
NM_001369.2(DNAH5):c.4687G>A (p.Gly1563Ser) rs147567352
NM_001369.2(DNAH5):c.4796+11C>A rs146696580
NM_001369.2(DNAH5):c.5114+11T>C rs6554820
NM_001369.2(DNAH5):c.5115-4G>T rs141141086
NM_001369.2(DNAH5):c.5115-5T>C rs4429853
NM_001369.2(DNAH5):c.5172C>T (p.Ala1724=) rs10041113
NM_001369.2(DNAH5):c.5224T>C (p.Leu1742=) rs35963491
NM_001369.2(DNAH5):c.5266G>A (p.Glu1756Lys) rs116524991
NM_001369.2(DNAH5):c.5272-15del rs35337694
NM_001369.2(DNAH5):c.5272-16_5272-15del rs35337694
NM_001369.2(DNAH5):c.5485-11A>G rs372860402
NM_001369.2(DNAH5):c.5658C>T (p.Tyr1886=) rs6880264
NM_001369.2(DNAH5):c.5707C>T (p.Leu1903=) rs7719896
NM_001369.2(DNAH5):c.58-13T>C rs115758625
NM_001369.2(DNAH5):c.5907T>C (p.Ala1969=) rs569572855
NM_001369.2(DNAH5):c.6061+10A>G rs77957856
NM_001369.2(DNAH5):c.6062-4G>A rs143392650
NM_001369.2(DNAH5):c.6249G>A (p.Met2083Ile) rs753614861
NM_001369.2(DNAH5):c.624C>T (p.Asn208=) rs139640247
NM_001369.2(DNAH5):c.6264C>T (p.Ala2088=) rs1348689
NM_001369.2(DNAH5):c.6305G>A (p.Arg2102His) rs876657782
NM_001369.2(DNAH5):c.6444+11C>T rs1348691
NM_001369.2(DNAH5):c.6444+8A>G rs1348690
NM_001369.2(DNAH5):c.6579+3A>G rs727502976
NM_001369.2(DNAH5):c.6579+6A>G rs141389162
NM_001369.2(DNAH5):c.6703T>G (p.Leu2235Val) rs115109673
NM_001369.2(DNAH5):c.6731A>T (p.Lys2244Met) rs187023993
NM_001369.2(DNAH5):c.6919G>A (p.Val2307Ile) rs74604638
NM_001369.2(DNAH5):c.6989-13T>C rs112344370
NM_001369.2(DNAH5):c.71G>A (p.Gly24Glu) rs1530496
NM_001369.2(DNAH5):c.7212T>C (p.Asp2404=) rs876657454
NM_001369.2(DNAH5):c.7274G>A (p.Arg2425His) rs35900306
NM_001369.2(DNAH5):c.7388A>G (p.Gln2463Arg) rs10078391
NM_001369.2(DNAH5):c.7468_7488del (p.Trp2490_Leu2496del) rs727502975
NM_001369.2(DNAH5):c.7502G>C (p.Arg2501Pro) rs78853309
NM_001369.2(DNAH5):c.7531C>T (p.Arg2511Trp) rs564040169
NM_001369.2(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124
NM_001369.2(DNAH5):c.8128G>A (p.Gly2710Ser) rs1219540537
NM_001369.2(DNAH5):c.8224+15G>A rs148099176
NM_001369.2(DNAH5):c.832del (p.Ala278fs) rs727502977
NM_001369.2(DNAH5):c.8387A>G (p.Asp2796Gly) rs727502974
NM_001369.2(DNAH5):c.8449-12T>C rs111313933
NM_001369.2(DNAH5):c.8586G>T (p.Leu2862Phe) rs10513155
NM_001369.2(DNAH5):c.8642C>G (p.Ala2881Gly) rs727502973
NM_001369.2(DNAH5):c.8840C>T (p.Thr2947Ile) rs756216163
NM_001369.2(DNAH5):c.8898G>A (p.Thr2966=) rs111995400
NM_001369.2(DNAH5):c.9449del (p.Gly3150fs) rs727504802
NM_001369.2(DNAH5):c.9522G>A (p.Thr3174=) rs35233147
NM_001369.2(DNAH5):c.9721-12A>T rs12655133

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