ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.4001T>C (p.Ile1334Thr) rs72657309 0.00171
NM_001277115.2(DNAH11):c.3466G>A (p.Gly1156Arg) rs183521702 0.00149
NM_001277115.2(DNAH11):c.2486G>A (p.Arg829His) rs201261243 0.00129
NM_001277115.2(DNAH11):c.7325A>G (p.Lys2442Arg) rs114286628 0.00080
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703 0.00079
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255 0.00069
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895 0.00048
NM_001277115.2(DNAH11):c.2682C>T (p.Leu894=) rs149926178 0.00031
NM_001277115.2(DNAH11):c.3853-5C>G rs367628980 0.00024
NM_001277115.2(DNAH11):c.2038G>A (p.Asp680Asn) rs201121146 0.00016
NM_001277115.2(DNAH11):c.9499A>C (p.Thr3167Pro) rs202224167 0.00014
NM_001277115.2(DNAH11):c.10631A>G (p.Glu3544Gly) rs928335497 0.00006
NM_001277115.2(DNAH11):c.1720A>G (p.Ile574Val) rs374359812 0.00006
NM_001277115.2(DNAH11):c.5622-7C>A rs727503901 0.00006
NM_001277115.2(DNAH11):c.1671A>C (p.Glu557Asp) rs764968620 0.00003
NM_001277115.2(DNAH11):c.5936T>C (p.Leu1979Pro) rs772070316 0.00003
NM_001277115.2(DNAH11):c.1220A>C (p.Asp407Ala) rs780042783 0.00002
NM_001277115.2(DNAH11):c.5501G>A (p.Arg1834His) rs750430725 0.00002
NM_001277115.2(DNAH11):c.571C>T (p.His191Tyr) rs562163349 0.00002
NM_001277115.2(DNAH11):c.10041T>A (p.Asn3347Lys) rs772016314 0.00001
NM_001277115.2(DNAH11):c.4294T>G (p.Leu1432Val) rs794727390 0.00001
NM_001277115.2(DNAH11):c.11691-19delinsTG rs373641344
NM_001277115.2(DNAH11):c.11691-20dup rs5882827
NM_001277115.2(DNAH11):c.11717C>G (p.Ala3906Gly) rs200664169
NM_001277115.2(DNAH11):c.12509C>G (p.Thr4170Ser) rs12537531
NM_001277115.2(DNAH11):c.2631C>A (p.Ile877=) rs1003575600
NM_001277115.2(DNAH11):c.7039A>G (p.Thr2347Ala) rs794727671
NM_001277115.2(DNAH11):c.9572C>T (p.Thr3191Ile) rs760597183
NM_001277115.2(DNAH11):c.9640G>A (p.Ala3214Thr) rs141979671

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