ClinVar Miner

Variants in gene MYH14 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
363 65 0 24 12 0 1 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 uncertain significance likely benign benign
pathogenic 0 1 0 0
uncertain significance 1 0 9 4
likely benign 0 9 0 24
benign 0 4 24 0

All variants with conflicting interpretations #

Total variants: 35
Download table as spreadsheet
HGVS dbSNP
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044
NM_001145809.2(MYH14):c.1275C>T (p.Thr425=) rs149221129
NM_001145809.2(MYH14):c.1427G>A (p.Arg476His)
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011
NM_001145809.2(MYH14):c.2680C>A (p.Arg894=) rs34805056
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437
NM_001145809.2(MYH14):c.3778G>A (p.Gly1260Ser) rs200272339
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006
NM_001145809.2(MYH14):c.4033G>A (p.Ala1345Thr) rs148054042
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.2(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5127+10G>A rs370928889
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.2(MYH14):c.565C>T (p.Arg189Cys) rs200818171
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634
NM_001145809.2(MYH14):c.5960+8C>T rs373176553
NM_001145809.2(MYH14):c.5964C>T (p.Arg1988=) rs768413723
NM_001145809.2(MYH14):c.615G>A (p.Thr205=) rs199921330
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295

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