ClinVar Miner

List of variants in gene DNAH11 reported as likely benign for not provided

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Gene type:
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Total variants: 95
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HGVS dbSNP
NM_001277115.2(DNAH11):c.1002T>C (p.Asp334=) rs370925563
NM_001277115.2(DNAH11):c.10176C>T (p.Arg3392=) rs370857029
NM_001277115.2(DNAH11):c.10379C>A (p.Thr3460Lys) rs573384750
NM_001277115.2(DNAH11):c.10620T>A (p.Ile3540=) rs1554284618
NM_001277115.2(DNAH11):c.10897-5A>G rs746604716
NM_001277115.2(DNAH11):c.11016G>A (p.Glu3672=) rs768633390
NM_001277115.2(DNAH11):c.1119T>C (p.Ser373=)
NM_001277115.2(DNAH11):c.11233G>A (p.Glu3745Lys) rs182389910
NM_001277115.2(DNAH11):c.11457C>T (p.Pro3819=) rs201185369
NM_001277115.2(DNAH11):c.11508C>T (p.Val3836=) rs199627577
NM_001277115.2(DNAH11):c.11712G>C (p.Leu3904=) rs761612271
NM_001277115.2(DNAH11):c.11883T>C (p.Asn3961=) rs1458288272
NM_001277115.2(DNAH11):c.11968-9A>C rs1018931263
NM_001277115.2(DNAH11):c.12057C>T (p.Phe4019=) rs200441507
NM_001277115.2(DNAH11):c.12066T>C (p.Ala4022=) rs1060504815
NM_001277115.2(DNAH11):c.12267C>T (p.Ala4089=) rs779248595
NM_001277115.2(DNAH11):c.12546C>T (p.Ala4182=) rs777625877
NM_001277115.2(DNAH11):c.12561T>G (p.Asp4187Glu) rs148429731
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703
NM_001277115.2(DNAH11):c.126G>A (p.Glu42=) rs748250611
NM_001277115.2(DNAH11):c.12735G>A (p.Gln4245=) rs1396708463
NM_001277115.2(DNAH11):c.12948A>G (p.Leu4316=) rs746607145
NM_001277115.2(DNAH11):c.13113G>T (p.Pro4371=) rs148707462
NM_001277115.2(DNAH11):c.13163-19T>A rs72658832
NM_001277115.2(DNAH11):c.13183C>A (p.Arg4395=) rs757784023
NM_001277115.2(DNAH11):c.1515C>T (p.His505=) rs773061951
NM_001277115.2(DNAH11):c.1545T>C (p.Cys515=) rs182332147
NM_001277115.2(DNAH11):c.1788G>A (p.Val596=) rs976690309
NM_001277115.2(DNAH11):c.180C>T (p.Arg60=) rs781089233
NM_001277115.2(DNAH11):c.2043A>G (p.Gln681=) rs375927648
NM_001277115.2(DNAH11):c.2115C>G (p.Pro705=) rs777633639
NM_001277115.2(DNAH11):c.2256A>G (p.Lys752=) rs775806737
NM_001277115.2(DNAH11):c.2349T>A (p.Pro783=) rs370930478
NM_001277115.2(DNAH11):c.2379C>T (p.Asp793=) rs375262840
NM_001277115.2(DNAH11):c.2409G>A (p.Leu803=) rs1048426613
NM_001277115.2(DNAH11):c.2664C>T (p.Val888=) rs757649943
NM_001277115.2(DNAH11):c.2682C>T (p.Leu894=) rs149926178
NM_001277115.2(DNAH11):c.2802A>G (p.Thr934=) rs755239180
NM_001277115.2(DNAH11):c.2824C>A (p.Pro942Thr) rs189569144
NM_001277115.2(DNAH11):c.3541A>G (p.Ser1181Gly) rs148916596
NM_001277115.2(DNAH11):c.3732C>T (p.Val1244=) rs1018800661
NM_001277115.2(DNAH11):c.3766-6G>T rs1209465431
NM_001277115.2(DNAH11):c.3786A>G (p.Arg1262=) rs756045492
NM_001277115.2(DNAH11):c.3843G>A (p.Ala1281=) rs374551688
NM_001277115.2(DNAH11):c.3946A>G (p.Met1316Val) rs17144788
NM_001277115.2(DNAH11):c.417A>C (p.Val139=) rs1583469182
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794
NM_001277115.2(DNAH11):c.459G>A (p.Ala153=) rs770376516
NM_001277115.2(DNAH11):c.4707G>C (p.Gly1569=) rs780784315
NM_001277115.2(DNAH11):c.4817+7A>T rs563875721
NM_001277115.2(DNAH11):c.4818-6A>T rs764444413
NM_001277115.2(DNAH11):c.4920C>T (p.Leu1640=) rs746563330
NM_001277115.2(DNAH11):c.5259T>C (p.Asp1753=) rs765453467
NM_001277115.2(DNAH11):c.5283G>C (p.Leu1761=) rs1060504813
NM_001277115.2(DNAH11):c.5329-9T>C rs773240082
NM_001277115.2(DNAH11):c.5625T>C (p.Cys1875=) rs368967707
NM_001277115.2(DNAH11):c.58C>A (p.Arg20Ser) rs72655967
NM_001277115.2(DNAH11):c.5904C>A (p.Ala1968=) rs756423819
NM_001277115.2(DNAH11):c.6143C>G (p.Thr2048Arg) rs184241449
NM_001277115.2(DNAH11):c.6387G>A (p.Arg2129=) rs1312853506
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys) rs140048925
NM_001277115.2(DNAH11):c.6437G>A (p.Arg2146His) rs727505321
NM_001277115.2(DNAH11):c.6594G>A (p.Pro2198=) rs200894470
NM_001277115.2(DNAH11):c.6810G>A (p.Leu2270=) rs774852383
NM_001277115.2(DNAH11):c.7126C>T (p.Leu2376=) rs549049467
NM_001277115.2(DNAH11):c.7134+10C>T rs757164819
NM_001277115.2(DNAH11):c.7209A>G (p.Glu2403=) rs1260213855
NM_001277115.2(DNAH11):c.7212C>T (p.Val2404=) rs777174573
NM_001277115.2(DNAH11):c.7257A>G (p.Leu2419=) rs1311166038
NM_001277115.2(DNAH11):c.7641G>A (p.Leu2547=) rs1247351644
NM_001277115.2(DNAH11):c.7725C>T (p.Ile2575=) rs1203442273
NM_001277115.2(DNAH11):c.7728C>T (p.Asp2576=) rs368846569
NM_001277115.2(DNAH11):c.7812-18C>G rs147865931
NM_001277115.2(DNAH11):c.794G>A (p.Arg265His) rs192989152
NM_001277115.2(DNAH11):c.798G>A (p.Leu266=) rs1583480795
NM_001277115.2(DNAH11):c.8040C>T (p.Pro2680=) rs1292903570
NM_001277115.2(DNAH11):c.8100G>T (p.Thr2700=) rs72657365
NM_001277115.2(DNAH11):c.8145C>T (p.Asn2715=) rs201592689
NM_001277115.2(DNAH11):c.8478C>T (p.His2826=) rs62445328
NM_001277115.2(DNAH11):c.864G>A (p.Leu288=) rs878854447
NM_001277115.2(DNAH11):c.8689T>C (p.Leu2897=) rs1583656714
NM_001277115.2(DNAH11):c.8766C>T (p.Phe2922=) rs752717335
NM_001277115.2(DNAH11):c.8797+3G>A rs772995648
NM_001277115.2(DNAH11):c.8969G>A (p.Arg2990His) rs72657371
NM_001277115.2(DNAH11):c.9039G>A (p.Ala3013=) rs373342289
NM_001277115.2(DNAH11):c.9303C>T (p.Asn3101=) rs375713138
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977
NM_001277115.2(DNAH11):c.93C>T (p.Gly31=) rs1219460682
NM_001277115.2(DNAH11):c.9561G>C (p.Leu3187=)
NM_001277115.2(DNAH11):c.9639C>T (p.Ile3213=) rs368831125
NM_001277115.2(DNAH11):c.9648C>T (p.Thr3216=) rs1583693853
NM_001277115.2(DNAH11):c.9663C>T (p.Ala3221=) rs566367592
NM_001277115.2(DNAH11):c.982+8T>A rs72655978
NM_001277115.2(DNAH11):c.990C>T (p.Leu330=) rs376448045
NM_001277115.2(DNAH11):c.9924+7A>G rs762368078

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