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 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
212 28 0 41 9 0 1 49

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 0 1 1
uncertain significance 0 0 8 2
likely benign 1 8 0 41
benign 1 2 41 0

All variants with conflicting interpretations #

Total variants: 49
Download table as spreadsheet
HGVS dbSNP
NM_001077186.1(MYH14):c.3369-3C>T rs78192108
NM_001145809.1(MYH14):c.1114+13C>T rs11666328
NM_001145809.1(MYH14):c.1115-4C>T rs142696359
NM_001145809.1(MYH14):c.1149T>C (p.Phe383=) rs61734424
NM_001145809.1(MYH14):c.1483-10G>A rs73061136
NM_001145809.1(MYH14):c.1755C>T (p.Gly585=) rs61731838
NM_001145809.1(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.1(MYH14):c.2205C>G (p.Arg735=) rs378811
NM_001145809.1(MYH14):c.2792G>A (p.Arg931His) rs200351672
NM_001145809.1(MYH14):c.2827-9A>C rs3745503
NM_001145809.1(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.1(MYH14):c.3680+9C>T rs76579307
NM_001145809.1(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363
NM_001145809.1(MYH14):c.4741G>A (p.Val1581Ile) rs680446
NM_001145809.1(MYH14):c.474T>C (p.Ile158=) rs34796700
NM_001145809.1(MYH14):c.4753-9C>T rs45591233
NM_001145809.1(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.1(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.1(MYH14):c.5573G>A (p.Arg1858His) rs11882073
NM_001145809.1(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_001145809.1(MYH14):c.91C>A (p.Pro31Thr) rs590722
NM_024729.3(MYH14):c.1000C>G (p.Pro334Ala) rs34498817
NM_024729.3(MYH14):c.1002G>A (p.Pro334=) rs368124508
NM_024729.3(MYH14):c.1010C>G (p.Ser337Cys) rs35315400
NM_024729.3(MYH14):c.1126G>T (p.Gly376Cys) rs119103280
NM_024729.3(MYH14):c.1181A>G (p.Asn394Ser) rs537153044
NM_024729.3(MYH14):c.1866C>T (p.Val622=) rs77895476
NM_024729.3(MYH14):c.2211C>A (p.Leu737=) rs190941610
NM_024729.3(MYH14):c.2236G>A (p.Glu746Lys) rs397516628
NM_024729.3(MYH14):c.2309C>T (p.Ala770Val) rs201337011
NM_024729.3(MYH14):c.2477G>A (p.Arg826His) rs547836952
NM_024729.3(MYH14):c.2718C>T (p.Arg906=) rs138987081
NM_024729.3(MYH14):c.2956C>T (p.Leu986=) rs113152264
NM_024729.3(MYH14):c.3414C>T (p.Ala1138=) rs559356437
NM_024729.3(MYH14):c.3540C>T (p.Asn1180=) rs78573213
NM_024729.3(MYH14):c.3626C>A (p.Ala1209Glu) rs11669191
NM_024729.3(MYH14):c.3655G>A (p.Gly1219Ser) rs200272339
NM_024729.3(MYH14):c.3748G>T (p.Val1250Leu) rs202242879
NM_024729.3(MYH14):c.3971G>A (p.Ser1324Asn) rs202225655
NM_024729.3(MYH14):c.4416+10C>T rs561531825
NM_024729.3(MYH14):c.4463G>A (p.Arg1488His) rs185232438
NM_024729.3(MYH14):c.4473C>T (p.Ala1491=) rs35453633
NM_024729.3(MYH14):c.4630-5A>G rs118097099
NM_024729.3(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_024729.3(MYH14):c.5211T>C (p.Gly1737=) rs115844649
NM_024729.3(MYH14):c.5343G>A (p.Leu1781=) rs10419343
NM_024729.3(MYH14):c.5406C>T (p.Ser1802=) rs12610591
NM_024729.3(MYH14):c.5889A>T (p.Leu1963=) rs73932457
NM_024729.3(MYH14):c.802A>G (p.Ile268Val) rs55645295

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.