ClinVar Miner

Variants in gene DNAH11 with conflicting interpretations

See also:
Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
1142 73 1 45 80 0 2 116

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 1 2 2 0 0
likely pathogenic 3 0 0 0 0
uncertain significance 2 0 0 35 47
likely benign 0 0 35 0 42
benign 0 0 47 42 0

All variants with conflicting interpretations #

Total variants: 116
Download table as spreadsheet
HGVS dbSNP
NM_001277115.2(DNAH11):c.10391C>T (p.Thr3464Ile) rs141112088
NM_001277115.2(DNAH11):c.10411G>A (p.Glu3471Lys) rs117729990
NM_001277115.2(DNAH11):c.10449C>T (p.Ala3483=) rs117000348
NM_001277115.2(DNAH11):c.1053G>A (p.Glu351=) rs201475447
NM_001277115.2(DNAH11):c.10573T>C (p.Leu3525=) rs886062182
NM_001277115.2(DNAH11):c.1065A>G (p.Pro355=) rs4392792
NM_001277115.2(DNAH11):c.10691+2T>C rs886039341
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400
NM_001277115.2(DNAH11):c.10976C>T (p.Ala3659Val) rs150631721
NM_001277115.2(DNAH11):c.11202+7C>A rs73279826
NM_001277115.2(DNAH11):c.11233G>A (p.Glu3745Lys) rs182389910
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.11374A>G (p.Ile3792Val) rs201700629
NM_001277115.2(DNAH11):c.11402C>G (p.Pro3801Arg) rs146362213
NM_001277115.2(DNAH11):c.11691-20dup rs5882827
NM_001277115.2(DNAH11):c.11805G>A (p.Pro3935=) rs187489343
NM_001277115.2(DNAH11):c.1199C>T (p.Thr400Ile) rs72655982
NM_001277115.2(DNAH11):c.12174C>T (p.Ala4058=) rs185794149
NM_001277115.2(DNAH11):c.12175G>A (p.Ala4059Thr) rs142372794
NM_001277115.2(DNAH11):c.12288G>A (p.Arg4096=) rs72658820
NM_001277115.2(DNAH11):c.12363C>G (p.Tyr4121Ter) rs121908855
NM_001277115.2(DNAH11):c.12509C>T (p.Thr4170Ile) rs12537531
NM_001277115.2(DNAH11):c.12534A>G (p.Pro4178=) rs752183095
NM_001277115.2(DNAH11):c.12561T>G (p.Asp4187Glu) rs148429731
NM_001277115.2(DNAH11):c.12601C>T (p.Pro4201Ser) rs200166341
NM_001277115.2(DNAH11):c.12632C>T (p.Pro4211Leu) rs142585703
NM_001277115.2(DNAH11):c.12899G>A (p.Arg4300His) rs377388499
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln) rs113653972
NM_001277115.2(DNAH11):c.13128C>A (p.Leu4376=) rs56333627
NM_001277115.2(DNAH11):c.13257A>G (p.Gly4419=) rs200445638
NM_001277115.2(DNAH11):c.1426-9T>C rs72655983
NM_001277115.2(DNAH11):c.1535T>A (p.Met512Lys) rs72655984
NM_001277115.2(DNAH11):c.1702G>A (p.Ala568Thr) rs72655988
NM_001277115.2(DNAH11):c.1749T>A (p.Val583=) rs368294823
NM_001277115.2(DNAH11):c.180C>T (p.Arg60=) rs781089233
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.1995C>T (p.His665=) rs752831166
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255
NM_001277115.2(DNAH11):c.2380G>A (p.Glu794Lys) rs78653098
NM_001277115.2(DNAH11):c.2419G>C (p.Asp807His) rs369849556
NM_001277115.2(DNAH11):c.2499C>T (p.Asn833=) rs201231307
NM_001277115.2(DNAH11):c.2682C>T (p.Leu894=) rs149926178
NM_001277115.2(DNAH11):c.2783A>T (p.Asp928Val) rs201386161
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.3237T>C (p.Leu1079=) rs72657304
NM_001277115.2(DNAH11):c.3256-10C>G rs17745898
NM_001277115.2(DNAH11):c.3384C>T (p.Ser1128=) rs79955190
NM_001277115.2(DNAH11):c.3425+5C>G rs776140118
NM_001277115.2(DNAH11):c.3853-5C>G rs367628980
NM_001277115.2(DNAH11):c.3946A>G (p.Met1316Val) rs17144788
NM_001277115.2(DNAH11):c.4095+2C>A rs532007878
NM_001277115.2(DNAH11):c.4124G>A (p.Arg1375His) rs151018293
NM_001277115.2(DNAH11):c.4202A>G (p.Gln1401Arg) rs199629774
NM_001277115.2(DNAH11):c.421G>T (p.Asp141Tyr) rs72655969
NM_001277115.2(DNAH11):c.4306C>T (p.Arg1436Trp) rs183489539
NM_001277115.2(DNAH11):c.4455A>G (p.Leu1485=) rs79119693
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794
NM_001277115.2(DNAH11):c.4598T>G (p.Ile1533Ser) rs73682656
NM_001277115.2(DNAH11):c.4713T>C (p.Asp1571=) rs72657324
NM_001277115.2(DNAH11):c.4904A>G (p.Asp1635Gly) rs17144835
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084
NM_001277115.2(DNAH11):c.5152A>G (p.Ile1718Val) rs137855415
NM_001277115.2(DNAH11):c.5359T>C (p.Leu1787=) rs75932225
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.5671C>T (p.Pro1891Ser) rs201704416
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met) rs72655972
NM_001277115.2(DNAH11):c.58C>A (p.Arg20Ser) rs72655967
NM_001277115.2(DNAH11):c.6117G>A (p.Ala2039=) rs78763603
NM_001277115.2(DNAH11):c.6274-5T>C rs74365849
NM_001277115.2(DNAH11):c.6302A>G (p.Asn2101Ser) rs201618995
NM_001277115.2(DNAH11):c.640A>G (p.Ile214Val) rs117064287
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.6607T>C (p.Leu2203=) rs202012891
NM_001277115.2(DNAH11):c.661A>T (p.Met221Leu) rs147525173
NM_001277115.2(DNAH11):c.6621T>A (p.Ala2207=) rs574427839
NM_001277115.2(DNAH11):c.6664C>T (p.Arg2222Ter) rs773498002
NM_001277115.2(DNAH11):c.6727C>T (p.Arg2243Ter) rs201943194
NM_001277115.2(DNAH11):c.7332G>A (p.Pro2444=) rs28370951
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.7626G>T (p.Thr2542=) rs2072221
NM_001277115.2(DNAH11):c.7756T>C (p.Tyr2586His) rs2003417
NM_001277115.2(DNAH11):c.7765G>A (p.Val2589Ile) rs145239537
NM_001277115.2(DNAH11):c.7800T>C (p.Asp2600=) rs774129338
NM_001277115.2(DNAH11):c.7812-18C>G rs147865931
NM_001277115.2(DNAH11):c.8023A>G (p.Ile2675Val) rs72657364
NM_001277115.2(DNAH11):c.8362C>G (p.His2788Asp) rs147478795
NM_001277115.2(DNAH11):c.8478C>T (p.His2826=) rs62445328
NM_001277115.2(DNAH11):c.8521A>G (p.Ser2841Gly) rs199789835
NM_001277115.2(DNAH11):c.8533C>G (p.Arg2845Gly) rs121908854
NM_001277115.2(DNAH11):c.8798-5G>A rs189821372
NM_001277115.2(DNAH11):c.891A>G (p.Ala297=) rs201934527
NM_001277115.2(DNAH11):c.8969G>A (p.Arg2990His) rs72657371
NM_001277115.2(DNAH11):c.8973G>A (p.Thr2991=) rs200978576
NM_001277115.2(DNAH11):c.8990G>A (p.Arg2997Gln) rs35865357
NM_001277115.2(DNAH11):c.9018G>A (p.Thr3006=) rs72657372
NM_001277115.2(DNAH11):c.9097A>G (p.Ile3033Val) rs72657373
NM_001277115.2(DNAH11):c.9098T>C (p.Ile3033Thr) rs28751578
NM_001277115.2(DNAH11):c.9102+8G>A rs72657374
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977
NM_001277115.2(DNAH11):c.9435G>A (p.Thr3145=) rs72657379
NM_001277115.2(DNAH11):c.9449G>A (p.Arg3150Gln) rs181785201
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) rs201207627
NM_001277115.2(DNAH11):c.9561G>A (p.Leu3187=) rs6965750
NM_001277115.2(DNAH11):c.9773A>G (p.Tyr3258Cys) rs182808328
NM_001277115.2(DNAH11):c.9925-7T>C rs146815254
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389
NM_001277115.2(DNAH11):c.9939G>A (p.Val3313=) rs200349268
NM_001277115.2(DNAH11):c.9966A>G (p.Gln3322=) rs201050208
Single allele

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