ClinVar Miner

List of variants in gene DNAH11 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.640A>G (p.Ile214Val) rs117064287 0.00595
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977 0.00522
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794 0.00461
NM_001277115.2(DNAH11):c.9435G>A (p.Thr3145=) rs72657379 0.00449
NM_001277115.2(DNAH11):c.8478C>T (p.His2826=) rs62445328 0.00419
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389 0.00307
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) rs201207627 0.00299
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400 0.00213
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln) rs113653972 0.00212
NM_001277115.2(DNAH11):c.4001T>C (p.Ile1334Thr) rs72657309 0.00171
NM_001277115.2(DNAH11):c.8533C>G (p.Arg2845Gly) rs121908854 0.00163
NM_001277115.2(DNAH11):c.3933A>G (p.Pro1311=) rs138071140 0.00153
NM_001277115.2(DNAH11):c.2486G>A (p.Arg829His) rs201261243 0.00129
NM_001277115.2(DNAH11):c.12174C>T (p.Ala4058=) rs185794149 0.00110
NM_001277115.2(DNAH11):c.13257A>G (p.Gly4419=) rs200445638 0.00103
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703 0.00079
NM_001277115.2(DNAH11):c.9110A>G (p.His3037Arg) rs192327380 0.00070
NM_001277115.2(DNAH11):c.4434C>T (p.His1478=) rs139082783 0.00052
NM_001277115.2(DNAH11):c.6352G>A (p.Gly2118Ser) rs72657342 0.00048
NM_001277115.2(DNAH11):c.8888C>A (p.Ser2963Tyr) rs374033085 0.00047
NM_001277115.2(DNAH11):c.569A>T (p.Tyr190Phe) rs201793112 0.00043
NM_001277115.2(DNAH11):c.8521A>G (p.Ser2841Gly) rs199789835 0.00042
NM_001277115.2(DNAH11):c.5671C>T (p.Pro1891Ser) rs201704416 0.00039
NM_001277115.2(DNAH11):c.11418C>T (p.Phe3806=) rs187814474 0.00036
NM_001277115.2(DNAH11):c.1749T>A (p.Val583=) rs368294823 0.00034
NM_001277115.2(DNAH11):c.8973G>A (p.Thr2991=) rs200978576 0.00028
NM_001277115.2(DNAH11):c.6264C>T (p.Pro2088=) rs187936691 0.00027
NM_001277115.2(DNAH11):c.661A>T (p.Met221Leu) rs147525173 0.00024
NM_001277115.2(DNAH11):c.11107G>C (p.Glu3703Gln) rs762297426 0.00023
NM_001277115.2(DNAH11):c.7365C>T (p.Asp2455=) rs183855253 0.00023
NM_001277115.2(DNAH11):c.9499A>C (p.Thr3167Pro) rs202224167 0.00014
NM_001277115.2(DNAH11):c.2826G>A (p.Pro942=) rs368794820 0.00011
NM_001277115.2(DNAH11):c.9039G>A (p.Ala3013=) rs373342289 0.00005
NM_001277115.2(DNAH11):c.882+7A>G rs533700730 0.00004
NM_001277115.2(DNAH11):c.8247A>G (p.Lys2749=) rs367806628 0.00003
NM_001277115.2(DNAH11):c.1995C>T (p.His665=) rs752831166 0.00001
NM_001277115.2(DNAH11):c.4491G>A (p.Glu1497=) rs564202359 0.00001
NM_001277115.2(DNAH11):c.1056G>C (p.Thr352=)
NM_001277115.2(DNAH11):c.12901A>G (p.Ile4301Val)
NM_001277115.2(DNAH11):c.13113G>C (p.Pro4371=) rs148707462
NM_001277115.2(DNAH11):c.13163-10_13163-7dup rs528000635
NM_001277115.2(DNAH11):c.2803G>A (p.Glu935Lys)
NM_001277115.2(DNAH11):c.4371T>A (p.Thr1457=)
NM_001277115.2(DNAH11):c.5262A>G (p.Val1754=)
NM_001277115.2(DNAH11):c.6987T>C (p.Tyr2329=)
NM_001277115.2(DNAH11):c.7140A>G (p.Leu2380=)
NM_001277115.2(DNAH11):c.7785C>T (p.Ile2595=)
NM_001277115.2(DNAH11):c.8023A>G (p.Ile2675Val) rs72657364
NM_001277115.2(DNAH11):c.9480A>T (p.Arg3160=)

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