ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance for not provided

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Total variants: 53
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HGVS dbSNP
GRCh37/hg19 7p15.3(chr7:21816449-21828046)x1
NM_001277115.2(DNAH11):c.10041T>A (p.Asn3347Lys) rs772016314
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895
NM_001277115.2(DNAH11):c.10631A>G (p.Glu3544Gly) rs928335497
NM_001277115.2(DNAH11):c.10691+2T>C rs886039341
NM_001277115.2(DNAH11):c.10780C>T (p.Pro3594Ser) rs746317366
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.1220A>C (p.Asp407Ala) rs780042783
NM_001277115.2(DNAH11):c.12264C>G (p.His4088Gln) rs368428210
NM_001277115.2(DNAH11):c.12509C>G (p.Thr4170Ser) rs12537531
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703
NM_001277115.2(DNAH11):c.13167_13177dup (p.Met4393fs) rs1583827297
NM_001277115.2(DNAH11):c.1459C>G (p.Leu487Val) rs759291863
NM_001277115.2(DNAH11):c.1671A>C (p.Glu557Asp) rs764968620
NM_001277115.2(DNAH11):c.1720A>G (p.Ile574Val) rs374359812
NM_001277115.2(DNAH11):c.180C>T (p.Arg60=) rs781089233
NM_001277115.2(DNAH11):c.2038G>A (p.Asp680Asn) rs201121146
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255
NM_001277115.2(DNAH11):c.2486G>A (p.Arg829His) rs201261243
NM_001277115.2(DNAH11):c.2631C>A (p.Ile877=) rs1003575600
NM_001277115.2(DNAH11):c.2682C>T (p.Leu894=) rs149926178
NM_001277115.2(DNAH11):c.3466G>A (p.Gly1156Arg) rs183521702
NM_001277115.2(DNAH11):c.3476G>A (p.Arg1159Lys) rs1192624503
NM_001277115.2(DNAH11):c.3853-5C>G rs367628980
NM_001277115.2(DNAH11):c.4000A>G (p.Ile1334Val) rs117965307
NM_001277115.2(DNAH11):c.4001T>C (p.Ile1334Thr) rs72657309
NM_001277115.2(DNAH11):c.4072G>A (p.Val1358Ile) rs483352711
NM_001277115.2(DNAH11):c.4294T>G (p.Leu1432Val) rs794727390
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084
NM_001277115.2(DNAH11):c.5501G>A (p.Arg1834His) rs750430725
NM_001277115.2(DNAH11):c.5528A>C (p.His1843Pro)
NM_001277115.2(DNAH11):c.5622-7C>A rs727503901
NM_001277115.2(DNAH11):c.571C>T (p.His191Tyr) rs562163349
NM_001277115.2(DNAH11):c.5936T>C (p.Leu1979Pro) rs772070316
NM_001277115.2(DNAH11):c.6302A>G (p.Asn2101Ser) rs201618995
NM_001277115.2(DNAH11):c.6352G>A (p.Gly2118Ser) rs72657342
NM_001277115.2(DNAH11):c.6376G>A (p.Val2126Met) rs772530809
NM_001277115.2(DNAH11):c.6566G>A (p.Arg2189Gln) rs747789567
NM_001277115.2(DNAH11):c.698C>T (p.Pro233Leu) rs776376992
NM_001277115.2(DNAH11):c.7039A>G (p.Thr2347Ala) rs794727671
NM_001277115.2(DNAH11):c.7325A>G (p.Lys2442Arg) rs114286628
NM_001277115.2(DNAH11):c.7360G>T (p.Val2454Leu)
NM_001277115.2(DNAH11):c.7915-6T>G
NM_001277115.2(DNAH11):c.8104A>G (p.Ile2702Val) rs760332753
NM_001277115.2(DNAH11):c.8279A>G (p.Gln2760Arg) rs72657366
NM_001277115.2(DNAH11):c.8335C>A (p.Leu2779Met) rs760409547
NM_001277115.2(DNAH11):c.8870C>G (p.Ala2957Gly) rs369875222
NM_001277115.2(DNAH11):c.9499A>C (p.Thr3167Pro) rs202224167
NM_001277115.2(DNAH11):c.9572C>T (p.Thr3191Ile) rs760597183
NM_001277115.2(DNAH11):c.9640G>A (p.Ala3214Thr) rs141979671
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389

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