ClinVar Miner

Variants in gene MYH9 with conflicting interpretations

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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
394 57 9 31 16 0 0 48

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 9 3 0 0 0
likely pathogenic 3 0 0 0 0
uncertain significance 0 0 0 16 6
likely benign 0 0 16 0 28
benign 0 0 6 28 0

All variants with conflicting interpretations #

Total variants: 48
Download table as spreadsheet
NM_002473.5(MYH9):c.1479G>A (p.Gln493=) rs376262583
NM_002473.5(MYH9):c.165C>T (p.Ile55=) rs141948797
NM_002473.5(MYH9):c.2104C>T (p.Arg702Cys) rs80338826
NM_002473.5(MYH9):c.2105G>A (p.Arg702His) rs80338827
NM_002473.5(MYH9):c.2871C>T (p.Ser957=) rs374840260
NM_002473.5(MYH9):c.287C>T (p.Ser96Leu) rs121913657
NM_002473.5(MYH9):c.3493C>T (p.Arg1165Cys) rs80338829
NM_002473.5(MYH9):c.4270G>A (p.Asp1424Asn) rs80338831
NM_002473.5(MYH9):c.4270G>C (p.Asp1424His) rs80338831
NM_002473.5(MYH9):c.4270G>T (p.Asp1424Tyr) rs80338831
NM_002473.5(MYH9):c.4340A>T (p.Asp1447Val) rs797044804
NM_002473.5(MYH9):c.5277C>T (p.Ile1759=) rs183105164
NM_002473.5(MYH9):c.543G>A (p.Thr181=) rs146514663
NM_002473.5(MYH9):c.5456T>G (p.Leu1819Arg) rs368440234
NM_002473.5(MYH9):c.5521G>A (p.Glu1841Lys) rs80338834
NM_002473.5(MYH9):c.5797C>T (p.Arg1933Ter) rs80338835
NM_002473.6(MYH9):c.1083C>T (p.Asp361=) rs56001030
NM_002473.6(MYH9):c.1158C>T (p.Thr386=) rs138502859
NM_002473.6(MYH9):c.1176G>A (p.Pro392=) rs143316848
NM_002473.6(MYH9):c.1242C>T (p.Ile414=) rs138436678
NM_002473.6(MYH9):c.1491C>T (p.Ile497=) rs146487404
NM_002473.6(MYH9):c.1566G>A (p.Pro522=) rs145517108
NM_002473.6(MYH9):c.1686G>A (p.Leu562=) rs199506577
NM_002473.6(MYH9):c.2061C>T (p.Leu687=) rs143801000
NM_002473.6(MYH9):c.2448C>T (p.Cys816=) rs113285582
NM_002473.6(MYH9):c.2517G>A (p.Gln839=) rs34498733
NM_002473.6(MYH9):c.2721C>T (p.Thr907=) rs148112044
NM_002473.6(MYH9):c.2872G>A (p.Ala958Thr) rs151036570
NM_002473.6(MYH9):c.3192C>T (p.Ile1064=) rs144807538
NM_002473.6(MYH9):c.3216G>A (p.Ala1072=) rs139441456
NM_002473.6(MYH9):c.3340T>C (p.Ser1114Pro) rs200901330
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635
NM_002473.6(MYH9):c.4225G>A (p.Asp1409Asn) rs34292387
NM_002473.6(MYH9):c.4344+10C>T rs200977419
NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727
NM_002473.6(MYH9):c.4818G>A (p.Ser1606=) rs202132383
NM_002473.6(MYH9):c.4878C>T (p.Ile1626=) rs143947828
NM_002473.6(MYH9):c.4952T>C (p.Met1651Thr) rs142094977
NM_002473.6(MYH9):c.4956C>T (p.Arg1652=) rs148632964
NM_002473.6(MYH9):c.5026A>G (p.Lys1676Glu) rs138158369
NM_002473.6(MYH9):c.5151-4G>A rs368125656
NM_002473.6(MYH9):c.5181G>A (p.Leu1727=) rs115170675
NM_002473.6(MYH9):c.5593-14G>T rs201676960
NM_002473.6(MYH9):c.5709C>T (p.Ala1903=) rs145444485
NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr) rs115031369
NM_002473.6(MYH9):c.5877C>T (p.Ala1959=) rs144179406
NM_002473.6(MYH9):c.591G>A (p.Ser197=) rs140241271
NM_002473.6(MYH9):c.7C>G (p.Gln3Glu) rs56200894

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