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 Variants with at least 2 submissions 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 kind of conflict
196 29 0 30 28 0 1 55

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 1 1 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 1 1 0 20 11
likely benign 0 0 20 0 29
benign 0 0 11 29 0

All variants with conflicting interpretations #

Total variants: 55
Download table as spreadsheet
HGVS dbSNP
NM_001083961.1(WDR62):c.*5G>A rs61740165
NM_001083961.1(WDR62):c.1228G>T (p.Val410Leu) rs139460397
NM_001083961.1(WDR62):c.1233+13C>T rs76130844
NM_001083961.1(WDR62):c.1233+15delC rs373693641
NM_001083961.1(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.1(WDR62):c.142C>T (p.Leu48Phe) rs62109744
NM_001083961.1(WDR62):c.1470C>T (p.Asp490=) rs45567532
NM_001083961.1(WDR62):c.1576G>A (p.Glu526Lys) rs147875659
NM_001083961.1(WDR62):c.1641G>A (p.Thr547=) rs2301734
NM_001083961.1(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.1(WDR62):c.1642+8C>T rs143309981
NM_001083961.1(WDR62):c.1643-10C>T rs4806263
NM_001083961.1(WDR62):c.1643-39G>A rs2301735
NM_001083961.1(WDR62):c.180G>A (p.Val60=) rs61742664
NM_001083961.1(WDR62):c.186C>T (p.Leu62=) rs11538454
NM_001083961.1(WDR62):c.2016C>T (p.Asp672=) rs114968951
NM_001083961.1(WDR62):c.2112G>C (p.Ser704=) rs115453534
NM_001083961.1(WDR62):c.2147-34G>A rs2301736
NM_001083961.1(WDR62):c.2211-4G>A rs202109439
NM_001083961.1(WDR62):c.2271G>A (p.Leu757=) rs61494900
NM_001083961.1(WDR62):c.2281C>T (p.His761Tyr) rs61744321
NM_001083961.1(WDR62):c.2334-29C>T rs2301737
NM_001083961.1(WDR62):c.2334-6C>A rs138928852
NM_001083961.1(WDR62):c.2529C>T (p.Asp843=) rs144697999
NM_001083961.1(WDR62):c.2549T>C (p.Leu850Ser) rs2285745
NM_001083961.1(WDR62):c.2666T>C (p.Met889Thr) rs139749569
NM_001083961.1(WDR62):c.269+12delA rs797046108
NM_001083961.1(WDR62):c.2766C>T (p.Arg922=) rs373906889
NM_001083961.1(WDR62):c.2975C>T (p.Ser992Leu) rs74518295
NM_001083961.1(WDR62):c.2976G>A (p.Ser992=) rs757294519
NM_001083961.1(WDR62):c.2991C>T (p.Ala997=) rs77898819
NM_001083961.1(WDR62):c.3033G>A (p.Pro1011=) rs118175551
NM_001083961.1(WDR62):c.3087C>T (p.Cys1029=) rs141344823
NM_001083961.1(WDR62):c.3231C>T (p.Pro1077=) rs187029707
NM_001083961.1(WDR62):c.3271_3273delCAC (p.His1091del) rs794727435
NM_001083961.1(WDR62):c.3303G>A (p.Thr1101=) rs117887683
NM_001083961.1(WDR62):c.3401T>G (p.Met1134Arg) rs61741470
NM_001083961.1(WDR62):c.3468C>T (p.Leu1156=) rs17851502
NM_001083961.1(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.1(WDR62):c.3639C>T (p.Ser1213=) rs45470992
NM_001083961.1(WDR62):c.3674G>A (p.Arg1225His) rs61743589
NM_001083961.1(WDR62):c.3763G>A (p.Val1255Ile) rs146180208
NM_001083961.1(WDR62):c.3786C>T (p.Gly1262=) rs148415080
NM_001083961.1(WDR62):c.3812C>T (p.Ala1271Val) rs111294536
NM_001083961.1(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.1(WDR62):c.4123G>A (p.Gly1375Ser) rs17851503
NM_001083961.1(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.1(WDR62):c.4296C>T (p.Leu1432=) rs765001215
NM_001083961.1(WDR62):c.4312-5T>G rs182467995
NM_001083961.1(WDR62):c.4338C>T (p.Thr1446=) rs149289227
NM_001083961.1(WDR62):c.477G>A (p.Ala159=) rs146485488
NM_001083961.1(WDR62):c.562-13C>T rs78138007
NM_001083961.1(WDR62):c.700-18C>T rs10423651
NM_001083961.1(WDR62):c.866A>G (p.Lys289Arg) rs12327568
NM_001083961.2(WDR62):c.1233+15dup rs373693641

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