ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP
NM_001369.2(DNAH5):c.10191A>G (p.Lys3397=) rs1250972452
NM_001369.2(DNAH5):c.10434T>C (p.Asp3478=) rs758443484
NM_001369.2(DNAH5):c.10437A>G (p.Ala3479=) rs139881808
NM_001369.2(DNAH5):c.10440G>A (p.Glu3480=) rs1485742988
NM_001369.2(DNAH5):c.10872+9T>G rs1580066952
NM_001369.2(DNAH5):c.11385G>A (p.Val3795=) rs921373580
NM_001369.2(DNAH5):c.11570+9G>C rs1206430080
NM_001369.2(DNAH5):c.11574T>C (p.Ser3858=) rs188088000
NM_001369.2(DNAH5):c.11586G>C (p.Pro3862=) rs755874851
NM_001369.2(DNAH5):c.11586G>T (p.Pro3862=) rs755874851
NM_001369.2(DNAH5):c.1182A>T (p.Thr394=) rs1580874077
NM_001369.2(DNAH5):c.11940G>A (p.Glu3980=) rs377018163
NM_001369.2(DNAH5):c.1198-8A>T rs1580867586
NM_001369.2(DNAH5):c.12072T>C (p.Tyr4024=) rs1375859408
NM_001369.2(DNAH5):c.12384C>T (p.Leu4128=) rs772828833
NM_001369.2(DNAH5):c.12720C>T (p.Thr4240=) rs756222017
NM_001369.2(DNAH5):c.12900G>A (p.Gln4300=) rs1313735230
NM_001369.2(DNAH5):c.13125+8G>A rs1579871092
NM_001369.2(DNAH5):c.1332C>T (p.Leu444=) rs375771650
NM_001369.2(DNAH5):c.13338+16C>T rs115271897
NM_001369.2(DNAH5):c.1371A>G (p.Pro457=) rs750936789
NM_001369.2(DNAH5):c.1431C>T (p.His477=) rs1028207982
NM_001369.2(DNAH5):c.1536+8A>G rs1580862932
NM_001369.2(DNAH5):c.1563G>A (p.Lys521=) rs1580853552
NM_001369.2(DNAH5):c.159C>G (p.Thr53=) rs773322142
NM_001369.2(DNAH5):c.192+7T>A rs1210630945
NM_001369.2(DNAH5):c.2028C>T (p.Leu676=) rs1358924801
NM_001369.2(DNAH5):c.2053-7C>T rs1325993261
NM_001369.2(DNAH5):c.2211C>T (p.Ser737=) rs878854455
NM_001369.2(DNAH5):c.2578-25_2578-17dup rs71600031
NM_001369.2(DNAH5):c.2578-25_2578-19dup rs71600031
NM_001369.2(DNAH5):c.2703A>T (p.Ile901=) rs1580744784
NM_001369.2(DNAH5):c.2931A>C (p.Thr977=) rs1469143674
NM_001369.2(DNAH5):c.299G>C (p.Gly100Ala) rs144236383
NM_001369.2(DNAH5):c.3390C>T (p.Thr1130=) rs1189840629
NM_001369.2(DNAH5):c.3417T>C (p.Asp1139=) rs376330483
NM_001369.2(DNAH5):c.3465C>T (p.Ala1155=) rs765054817
NM_001369.2(DNAH5):c.3747C>T (p.Asp1249=) rs1280894186
NM_001369.2(DNAH5):c.3753T>C (p.Asp1251=) rs1060504237
NM_001369.2(DNAH5):c.3777G>C (p.Ala1259=) rs144893234
NM_001369.2(DNAH5):c.3861T>C (p.Tyr1287=) rs764026489
NM_001369.2(DNAH5):c.390C>T (p.Phe130=) rs1580909350
NM_001369.2(DNAH5):c.4023T>C (p.Asp1341=) rs148451151
NM_001369.2(DNAH5):c.438+8G>A rs950201438
NM_001369.2(DNAH5):c.489T>C (p.Ser163=) rs1580903831
NM_001369.2(DNAH5):c.5199G>A (p.Ser1733=) rs142806046
NM_001369.2(DNAH5):c.5272-33dup rs35337694
NM_001369.2(DNAH5):c.5272-9C>T rs555481241
NM_001369.2(DNAH5):c.5622C>T (p.Thr1874=) rs759459740
NM_001369.2(DNAH5):c.5814G>A (p.Val1938=) rs1580512154
NM_001369.2(DNAH5):c.5853C>T (p.Asp1951=) rs1475309331
NM_001369.2(DNAH5):c.6061+7G>C rs1334799290
NM_001369.2(DNAH5):c.6062-6T>C rs1471313971
NM_001369.2(DNAH5):c.6579+20G>A rs115382993
NM_001369.2(DNAH5):c.6672A>G (p.Ala2224=) rs1060504236
NM_001369.2(DNAH5):c.6703T>G (p.Leu2235Val) rs115109673
NM_001369.2(DNAH5):c.6919G>A (p.Val2307Ile) rs74604638
NM_001369.2(DNAH5):c.7167C>T (p.Thr2389=) rs377435331
NM_001369.2(DNAH5):c.7212T>C (p.Asp2404=) rs876657454
NM_001369.2(DNAH5):c.7231-9A>C rs945527843
NM_001369.2(DNAH5):c.7408-4T>C rs1388754784
NM_001369.2(DNAH5):c.741T>C (p.Pro247=) rs374902528
NM_001369.2(DNAH5):c.7560G>T (p.Pro2520=) rs762130845
NM_001369.2(DNAH5):c.7569G>A (p.Gly2523=) rs986872979
NM_001369.2(DNAH5):c.7581C>T (p.Thr2527=) rs1047174806
NM_001369.2(DNAH5):c.8011-4G>A rs1331845041
NM_001369.2(DNAH5):c.8388T>C (p.Asp2796=) rs1580265726
NM_001369.2(DNAH5):c.8685A>G (p.Lys2895=) rs553405333
NM_001369.2(DNAH5):c.8898G>T (p.Thr2966=) rs111995400
NM_001369.2(DNAH5):c.9111T>C (p.Ser3037=) rs765029802
NM_001369.2(DNAH5):c.9171A>G (p.Lys3057=) rs543154987
NM_001369.2(DNAH5):c.9210G>C (p.Leu3070=) rs1580176858
NM_001369.2(DNAH5):c.9605+7G>A rs1433603838
NM_001369.2(DNAH5):c.9810G>A (p.Val3270=) rs779435246
NM_001369.2(DNAH5):c.9825A>G (p.Lys3275=) rs1580139912
NM_001369.2(DNAH5):c.9879G>A (p.Glu3293=) rs764348016
NM_001369.2(DNAH5):c.9912G>C (p.Ser3304=) rs188218914

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