ClinVar Miner

Variants in gene ANO5 with conflicting interpretations

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
496 103 6 28 30 0 9 67

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 6 9 3 0 0
likely pathogenic 9 0 7 1 0
uncertain significance 3 7 0 24 8
likely benign 0 1 24 0 19
benign 0 0 8 19 0

All variants with conflicting interpretations #

Total variants: 67
Download table as spreadsheet
HGVS dbSNP
NM_213599.2(ANO5):c.*1286G>T rs7925081
NM_213599.2(ANO5):c.*1313A>G rs73483432
NM_213599.2(ANO5):c.*1328C>T rs78089375
NM_213599.2(ANO5):c.*1429A>G rs78143145
NM_213599.2(ANO5):c.*1521T>C rs73483433
NM_213599.2(ANO5):c.*1661C>T rs12284506
NM_213599.2(ANO5):c.*1712T>C rs530413127
NM_213599.2(ANO5):c.*2095G>A rs142192440
NM_213599.2(ANO5):c.*2357A>T rs151218419
NM_213599.2(ANO5):c.*279G>A rs72982058
NM_213599.2(ANO5):c.*2869A>G rs115249135
NM_213599.2(ANO5):c.*3152G>A rs79486036
NM_213599.2(ANO5):c.*3155T>C rs78929863
NM_213599.2(ANO5):c.*3168C>T rs35892535
NM_213599.2(ANO5):c.*3350T>G rs144806967
NM_213599.2(ANO5):c.*496A>G rs10766930
NM_213599.2(ANO5):c.*554C>T rs117180492
NM_213599.2(ANO5):c.*930C>T rs78428314
NM_213599.2(ANO5):c.-217G>T rs73479393
NM_213599.2(ANO5):c.-261A>C rs114897158
NM_213599.2(ANO5):c.1066T>C (p.Cys356Arg) rs119103234
NM_213599.2(ANO5):c.1066T>G (p.Cys356Gly) rs119103234
NM_213599.2(ANO5):c.1095A>G (p.Leu365=) rs35804601
NM_213599.2(ANO5):c.1120-24A>T rs11026476
NM_213599.2(ANO5):c.1222C>T (p.Leu408=) rs997655691
NM_213599.2(ANO5):c.1295C>G (p.Ala432Gly) rs137854524
NM_213599.2(ANO5):c.1362G>A (p.Thr454=) rs747933251
NM_213599.2(ANO5):c.138+10G>A rs78987921
NM_213599.2(ANO5):c.139-1del rs868484837
NM_213599.2(ANO5):c.1391C>A (p.Ala464Asp) rs529961953
NM_213599.2(ANO5):c.1538C>T (p.Thr513Ile) rs281865467
NM_213599.2(ANO5):c.1545A>G (p.Ser515=) rs35843353
NM_213599.2(ANO5):c.155A>G rs143777403
NM_213599.2(ANO5):c.1664G>T (p.Ser555Ile) rs375014127
NM_213599.2(ANO5):c.169C>T (p.Arg57Trp) rs1323349209
NM_213599.2(ANO5):c.172C>T (p.Arg58Trp) rs201725369
NM_213599.2(ANO5):c.191dupA rs137854521
NM_213599.2(ANO5):c.2139C>T (p.Thr713=) rs767479331
NM_213599.2(ANO5):c.2176dup (p.Ser726fs) rs797044667
NM_213599.2(ANO5):c.2236-13_2236-10del rs72105710
NM_213599.2(ANO5):c.2256G>A (p.Thr752=) rs144048656
NM_213599.2(ANO5):c.2259A>G (p.Ser753=) rs61746201
NM_213599.2(ANO5):c.2354T>G (p.Leu785Arg) rs146136277
NM_213599.2(ANO5):c.2387C>T (p.Ser796Leu) rs61910685
NM_213599.2(ANO5):c.242A>G (p.Asp81Gly) rs199501657
NM_213599.2(ANO5):c.2498T>A (p.Met833Lys) rs142073798
NM_213599.2(ANO5):c.2503_2505del (p.Phe835del) rs794727350
NM_213599.2(ANO5):c.2521C>G (p.His841Asp) rs781027702
NM_213599.2(ANO5):c.259G>A (p.Val87Ile) rs34994927
NM_213599.2(ANO5):c.2610A>G (p.Leu870=) rs369103376
NM_213599.2(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.2(ANO5):c.2688C>G (p.Ala896=) rs377549896
NM_213599.2(ANO5):c.2698A>C (p.Met900Leu) rs148293985
NM_213599.2(ANO5):c.276A>G (p.Lys92=) rs201678262
NM_213599.2(ANO5):c.295-8dup rs778435515
NM_213599.2(ANO5):c.364-8del rs146983312
NM_213599.2(ANO5):c.41-1G>A rs398124625
NM_213599.2(ANO5):c.616A>G (p.Thr206Ala) rs78266558
NM_213599.2(ANO5):c.680G>C (p.Gly227Ala) rs140903276
NM_213599.2(ANO5):c.692G>T (p.Gly231Val) rs137854523
NM_213599.2(ANO5):c.69C>A (p.Tyr23Ter) rs762035813
NM_213599.2(ANO5):c.720G>T (p.Leu240=) rs147121216
NM_213599.2(ANO5):c.879-7_879-6del rs143977836
NM_213599.3(ANO5):c.1029C>T (p.Asp343=) rs78899595
NM_213599.3(ANO5):c.2272C>T (p.Arg758Cys) rs137854529
NM_213599.3(ANO5):c.2311_2312del (p.Gln771fs) rs137854528
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.