ClinVar Miner

Variants in gene PRX 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 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
375 61 3 22 33 0 12 63

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 3 0 11 0 0
likely pathogenic 0 0 1 0 0
uncertain significance 11 1 0 27 11
likely benign 0 0 27 0 22
benign 0 0 11 22 0

All variants with conflicting interpretations #

Total variants: 63
Download table as spreadsheet
HGVS dbSNP
NM_020956.2(PRX):c.*1028C>A rs200033507
NM_020956.2(PRX):c.*1097C>T rs185112635
NM_020956.2(PRX):c.*1165G>A rs775367319
NM_020956.2(PRX):c.*1256C>T rs73933276
NM_020956.2(PRX):c.*1295C>T
NM_020956.2(PRX):c.*1307C>T rs104894715
NM_020956.2(PRX):c.*1379C>T rs773009397
NM_020956.2(PRX):c.*1399_*1402del
NM_020956.2(PRX):c.*1421G>A rs117336941
NM_020956.2(PRX):c.*1486C>T rs76960467
NM_020956.2(PRX):c.*1705A>G rs777104457
NM_020956.2(PRX):c.*1779T>C rs149715830
NM_020956.2(PRX):c.*1830G>A rs139586219
NM_020956.2(PRX):c.*1856G>A rs61733448
NM_020956.2(PRX):c.*2041C>T rs574899855
NM_020956.2(PRX):c.*2156G>A rs3814290
NM_020956.2(PRX):c.*2169C>T rs118003416
NM_020956.2(PRX):c.*2222A>G rs61735531
NM_020956.2(PRX):c.*2248C>T rs56743160
NM_020956.2(PRX):c.*2303del rs281865062
NM_020956.2(PRX):c.*2350T>A rs104894707
NM_020956.2(PRX):c.*2369A>G rs376309142
NM_020956.2(PRX):c.*2459G>A rs147587689
NM_020956.2(PRX):c.*2850T>C rs268671
NM_020956.2(PRX):c.*2860T>C rs268672
NM_020956.2(PRX):c.*2894C>T
NM_020956.2(PRX):c.*2932C>T rs61735546
NM_020956.2(PRX):c.*2968A>G rs268673
NM_020956.2(PRX):c.*2980C>T rs201792838
NM_020956.2(PRX):c.*3315A>G rs148600818
NM_020956.2(PRX):c.*3350G>A rs186086914
NM_020956.2(PRX):c.*3391G>T rs139188673
NM_020956.2(PRX):c.*3413C>T rs104894708
NM_020956.2(PRX):c.*3423A>G rs61733451
NM_020956.2(PRX):c.*3453C>G rs3745202
NM_020956.2(PRX):c.*3578G>A rs148939995
NM_020956.2(PRX):c.*3599G>A rs268674
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*3754C>T rs367876251
NM_020956.2(PRX):c.*3907C>T rs139950446
NM_020956.2(PRX):c.*3980G>A rs751742049
NM_020956.2(PRX):c.*4007G>C rs146061247
NM_020956.2(PRX):c.*4051G>A rs143289108
NM_020956.2(PRX):c.*4057C>T rs567324732
NM_020956.2(PRX):c.*4152C>T rs142762689
NM_020956.2(PRX):c.*4249G>C rs76088917
NM_020956.2(PRX):c.*4264_*4266GGA[5] rs139624657
NM_020956.2(PRX):c.*590_*599dup
NM_020956.2(PRX):c.*650G>A rs142436391
NM_020956.2(PRX):c.*698C>T rs555499679
NM_020956.2(PRX):c.*704C>T rs10425452
NM_020956.2(PRX):c.*759G>A rs76756143
NM_020956.2(PRX):c.*791C>T rs104894706
NM_020956.2(PRX):c.*802C>T rs144157275
NM_020956.2(PRX):c.*888G>A rs562108874
NM_020956.2(PRX):c.*936C>T rs118071705
NM_020956.2(PRX):c.-20A>C rs780315081
NM_020956.2(PRX):c.-236G>A rs552436076
NM_020956.2(PRX):c.133C>G (p.Arg45Gly) rs115090201
NM_020956.2(PRX):c.237C>T (p.Asp79=) rs376174896
NM_020956.2(PRX):c.247del (p.Leu83fs) rs281865061
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_181882.3(PRX):c.3873C>G (p.Tyr1291Ter)

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