ClinVar Miner

List of variants in gene DNAH11 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 33
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HGVS dbSNP
NM_001277115.2(DNAH11):c.1065A>G (p.Pro355=) rs4392792
NM_001277115.2(DNAH11):c.11202+13G>A rs73279830
NM_001277115.2(DNAH11):c.11202+7C>A rs73279826
NM_001277115.2(DNAH11):c.11272T>C (p.Ser3758Pro) rs17145720
NM_001277115.2(DNAH11):c.11325G>A (p.Ala3775=) rs12666072
NM_001277115.2(DNAH11):c.1199C>T (p.Thr400Ile) rs72655982
NM_001277115.2(DNAH11):c.12288G>A (p.Arg4096=) rs72658820
NM_001277115.2(DNAH11):c.12508-12T>C rs72658822
NM_001277115.2(DNAH11):c.12509C>T (p.Thr4170Ile) rs12537531
NM_001277115.2(DNAH11):c.13128C>A (p.Leu4376=) rs56333627
NM_001277115.2(DNAH11):c.1702G>A (p.Ala568Thr) rs72655988
NM_001277115.2(DNAH11):c.1885C>T (p.Pro629Ser) rs150966144
NM_001277115.2(DNAH11):c.1916A>G (p.Gln639Arg) rs12670130
NM_001277115.2(DNAH11):c.1961C>G (p.Ser654Cys) rs62441683
NM_001277115.2(DNAH11):c.2275-15G>T rs60290948
NM_001277115.2(DNAH11):c.2835A>G (p.Gln945=) rs17144747
NM_001277115.2(DNAH11):c.3068T>C (p.Val1023Ala) rs10269582
NM_001277115.2(DNAH11):c.3105G>A (p.Glu1035=) rs191011620
NM_001277115.2(DNAH11):c.3256-10C>G rs17745898
NM_001277115.2(DNAH11):c.421G>T (p.Asp141Tyr) rs72655969
NM_001277115.2(DNAH11):c.4726-15T>C rs17144822
NM_001277115.2(DNAH11):c.4904A>G (p.Asp1635Gly) rs17144835
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=) rs55666134
NM_001277115.2(DNAH11):c.54C>T (p.Thr18=) rs2285942
NM_001277115.2(DNAH11):c.5621+11A>T rs59447021
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met) rs72655972
NM_001277115.2(DNAH11):c.6117G>A (p.Ala2039=) rs78763603
NM_001277115.2(DNAH11):c.7335G>A (p.Ser2445=) rs11768670
NM_001277115.2(DNAH11):c.7570T>C (p.Leu2524=) rs2072220
NM_001277115.2(DNAH11):c.7756T>C (p.Tyr2586His) rs2003417
NM_001277115.2(DNAH11):c.9098T>C (p.Ile3033Thr) rs28751578
NM_001277115.2(DNAH11):c.9561G>A (p.Leu3187=) rs6965750
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389

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