ClinVar Miner

Variants in gene MYPN 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
634 77 0 21 15 0 5 35

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 2 4 2 1
likely pathogenic 2 0 3 1 1
uncertain significance 4 3 0 15 2
likely benign 2 1 15 0 20
benign 1 1 2 20 0

All variants with conflicting interpretations #

Total variants: 35
Download table as spreadsheet
NM_032578.3(MYPN):c.1245+20A>G rs111634581
NM_032578.3(MYPN):c.1246-19G>A rs75739924
NM_032578.3(MYPN):c.2925+20A>C rs200111945
NM_032578.3(MYPN):c.3075+20C>T rs377273417
NM_032578.4(MYPN):c.1104C>T (p.Gly368=) rs144764983
NM_032578.4(MYPN):c.1122G>A (p.Glu374=) rs145103325
NM_032578.4(MYPN):c.1130G>A (p.Arg377Gln) rs147596628
NM_032578.4(MYPN):c.1134C>T (p.Ile378=) rs145701607
NM_032578.4(MYPN):c.1236C>A (p.Thr412=) rs151220474
NM_032578.4(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.4(MYPN):c.1460-14T>A rs201156035
NM_032578.4(MYPN):c.1790G>A (p.Arg597His) rs150911078
NM_032578.4(MYPN):c.1875C>G (p.Pro625=) rs2673793
NM_032578.4(MYPN):c.1893G>A (p.Arg631=) rs145440469
NM_032578.4(MYPN):c.1935C>T (p.Pro645=) rs71535754
NM_032578.4(MYPN):c.2236A>G (p.Thr746Ala) rs147287437
NM_032578.4(MYPN):c.2260A>C (p.Ile754Leu) rs201245117
NM_032578.4(MYPN):c.2863C>T (p.Arg955Trp) rs149887823
NM_032578.4(MYPN):c.2880T>G (p.Ser960=) rs146028308
NM_032578.4(MYPN):c.2882C>T (p.Pro961Leu) rs864621995
NM_032578.4(MYPN):c.2925+9G>C rs12241644
NM_032578.4(MYPN):c.3122T>A (p.Ile1041Asn) rs754227127
NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys) rs151282801
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_032578.4(MYPN):c.3417C>T (p.Arg1139=) rs144488384
NM_032578.4(MYPN):c.3456C>T (p.Thr1152=) rs202183926
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730
NM_032578.4(MYPN):c.3583G>A (p.Val1195Met) rs71534280
NM_032578.4(MYPN):c.3768G>A (p.Ser1256=) rs533708375
NM_032578.4(MYPN):c.392G>T (p.Ser131Ile) rs199853307
NM_032578.4(MYPN):c.3934C>T (p.Arg1312Trp) rs142354704
NM_032578.4(MYPN):c.410G>C (p.Arg137Thr) rs765931465
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys) rs140148105
NM_032578.4(MYPN):c.65C>G (p.Ala22Gly) rs145142157
NM_032578.4(MYPN):c.935C>T (p.Ser312Phe) rs786205457

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