ClinVar Miner

Variants in gene WDR62 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
308 49 0 29 27 0 3 52

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 0 0 2 0 0
likely pathogenic 0 0 2 0 0
uncertain significance 2 2 0 24 10
likely benign 0 0 24 0 29
benign 0 0 10 29 0

All variants with conflicting interpretations #

Total variants: 52
Download table as spreadsheet
NM_001083961.2(WDR62):c.*5G>A rs61740165
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) rs139460397
NM_001083961.2(WDR62):c.1233+15del rs373693641
NM_001083961.2(WDR62):c.1233+15dup rs373693641
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) rs62109744
NM_001083961.2(WDR62):c.1480G>A (p.Gly494Arg) rs587784543
NM_001083961.2(WDR62):c.1509C>T (p.Asp503=) rs758922011
NM_001083961.2(WDR62):c.1521G>A (p.Leu507=) rs778207666
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) rs147875659
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1643-39G>A rs2301735
NM_001083961.2(WDR62):c.1768+28G>A rs77938609
NM_001083961.2(WDR62):c.1769-7C>T rs137919897
NM_001083961.2(WDR62):c.189G>T (p.Glu63Asp) rs201053854
NM_001083961.2(WDR62):c.2016C>T (p.Asp672=) rs114968951
NM_001083961.2(WDR62):c.2040T>C (p.His680=) rs765451882
NM_001083961.2(WDR62):c.2112G>C (p.Ser704=) rs115453534
NM_001083961.2(WDR62):c.2147-34G>A rs2301736
NM_001083961.2(WDR62):c.2211-4G>A rs202109439
NM_001083961.2(WDR62):c.2334-29C>T rs2301737
NM_001083961.2(WDR62):c.2334-6C>A rs138928852
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=) rs144697999
NM_001083961.2(WDR62):c.2666T>C (p.Met889Thr) rs139749569
NM_001083961.2(WDR62):c.269+12del rs797046108
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=) rs373906889
NM_001083961.2(WDR62):c.2975C>T (p.Ser992Leu) rs74518295
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=) rs757294519
NM_001083961.2(WDR62):c.2991C>T (p.Ala997=) rs77898819
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=) rs118175551
NM_001083961.2(WDR62):c.303C>A (p.Asn101Lys) rs139371621
NM_001083961.2(WDR62):c.3087C>T (p.Cys1029=) rs141344823
NM_001083961.2(WDR62):c.3271_3273del (p.His1091del) rs794727435
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) rs117887683
NM_001083961.2(WDR62):c.3514+44G>A rs45468494
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) rs146180208
NM_001083961.2(WDR62):c.3786C>T (p.Gly1262=) rs148415080
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) rs111294536
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.2(WDR62):c.4033C>T (p.Arg1345Cys) rs201363122
NM_001083961.2(WDR62):c.4122C>T (p.Gly1374=) rs773948810
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.2(WDR62):c.4312-5T>G rs182467995
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=) rs149289227
NM_001083961.2(WDR62):c.477G>A (p.Ala159=) rs146485488
NM_001083961.2(WDR62):c.525C>T (p.Tyr175=) rs779093591
NM_001083961.2(WDR62):c.700-18C>T rs10423651
NM_001083961.2(WDR62):c.744C>T (p.Gly248=) rs146898747
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) rs12327568
NM_001083961.2(WDR62):c.875A>C (p.Asn292Thr) rs776948954

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.