ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 184
Download table as spreadsheet
HGVS dbSNP
NM_001040113.2(MYH11):c.5813C>A (p.Pro1938His) rs765030635
NM_001040113.2(MYH11):c.5819C>T (p.Pro1940Leu) rs111588143
NM_002474.3(MYH11):c.*13A>G rs191562149
NM_002474.3(MYH11):c.*19G>A rs187644296
NM_002474.3(MYH11):c.*5C>G rs1875184
NM_002474.3(MYH11):c.3700G>A (p.Ala1234Thr) rs16967494
NM_002474.3(MYH11):c.3859-206C>T rs760023
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala) rs16967510
NM_002474.3(MYH11):c.3891C>T (p.Asn1297=) rs541280738
NM_002474.3(MYH11):c.3895G>A (p.Ala1299Thr) rs1388360113
NM_002474.3(MYH11):c.3927C>T (p.Asp1309=) rs150712107
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3932C>T (p.Ala1311Val) rs185720909
NM_002474.3(MYH11):c.3933G>A (p.Ala1311=) rs78857360
NM_002474.3(MYH11):c.3949C>A (p.Leu1317Ile) rs141159831
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=) rs12907
NM_002474.3(MYH11):c.3973C>G (p.Gln1325Glu) rs150033906
NM_002474.3(MYH11):c.4016G>A (p.Arg1339His) rs374271463
NM_002474.3(MYH11):c.4068G>A (p.Met1356Ile) rs794728663
NM_002474.3(MYH11):c.4078C>G (p.Gln1360Glu) rs1555553235
NM_002474.3(MYH11):c.4095C>T (p.His1365=) rs374454281
NM_002474.3(MYH11):c.4116+11del rs543763112
NM_002474.3(MYH11):c.4116+12G>A rs193005461
NM_002474.3(MYH11):c.4117-14C>T rs374648974
NM_002474.3(MYH11):c.4117-44C>T rs11130
NM_002474.3(MYH11):c.4158C>T (p.Thr1386=) rs112377790
NM_002474.3(MYH11):c.4177G>C (p.Gly1393Arg) rs143620567
NM_002474.3(MYH11):c.4197G>A (p.Lys1399=) rs113302393
NM_002474.3(MYH11):c.4203C>T (p.Ile1401=) rs760611400
NM_002474.3(MYH11):c.4236G>A (p.Ala1412=) rs771460474
NM_002474.3(MYH11):c.4240G>A (p.Ala1414Thr) rs112467954
NM_002474.3(MYH11):c.4240_4242delinsACG (p.Ala1414Thr) rs794728676
NM_002474.3(MYH11):c.4242T>A (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4293C>T (p.Asp1431=) rs143588920
NM_002474.3(MYH11):c.4296G>A (p.Leu1432=)
NM_002474.3(MYH11):c.4303G>A (p.Asp1435Asn) rs794728668
NM_002474.3(MYH11):c.4319G>A (p.Arg1440Gln) rs763467593
NM_002474.3(MYH11):c.4345A>C (p.Lys1449Gln) rs775809843
NM_002474.3(MYH11):c.4365+23C>T rs7193920
NM_002474.3(MYH11):c.4365+310A>G
NM_002474.3(MYH11):c.4366-131T>C
NM_002474.3(MYH11):c.4374C>T (p.Ala1458=) rs767066866
NM_002474.3(MYH11):c.4401C>T (p.Tyr1467=) rs8046180
NM_002474.3(MYH11):c.4403C>T (p.Ala1468Val) rs370240337
NM_002474.3(MYH11):c.4418G>T (p.Arg1473Ile) rs758663266
NM_002474.3(MYH11):c.4459_4464del (p.Ser1487_Leu1488del) rs1555552158
NM_002474.3(MYH11):c.4506C>T (p.Leu1502=) rs76890940
NM_002474.3(MYH11):c.4522A>G (p.Met1508Val) rs35176378
NM_002474.3(MYH11):c.4538T>A (p.Met1513Lys) rs794728669
NM_002474.3(MYH11):c.4561G>A (p.Asp1521Asn) rs794728679
NM_002474.3(MYH11):c.4578+19T>C rs118072250
NM_002474.3(MYH11):c.4578+1G>A rs397514037
NM_002474.3(MYH11):c.4578+2dup rs794728677
NM_002474.3(MYH11):c.4578+3A>G rs143288748
NM_002474.3(MYH11):c.4578+5G>C rs1555552121
NM_002474.3(MYH11):c.4579-13G>A rs181115969
NM_002474.3(MYH11):c.4579-140T>C
NM_002474.3(MYH11):c.4579-14C>T rs377410503
NM_002474.3(MYH11):c.4579-29T>C
NM_002474.3(MYH11):c.4579-6C>T rs200223639
NM_002474.3(MYH11):c.4603C>T (p.Arg1535Trp) rs143402648
NM_002474.3(MYH11):c.4604G>A (p.Arg1535Gln) rs137934837
NM_002474.3(MYH11):c.4632G>C (p.Met1544Ile) rs1064797005
NM_002474.3(MYH11):c.4659C>T (p.Asp1553=) rs141031021
NM_002474.3(MYH11):c.4673C>T (p.Thr1558Met) rs111854563
NM_002474.3(MYH11):c.4674G>A (p.Thr1558=) rs778499852
NM_002474.3(MYH11):c.4680C>T (p.Asp1560=) rs142613263
NM_002474.3(MYH11):c.4717A>G (p.Lys1573Glu) rs151101824
NM_002474.3(MYH11):c.4735G>A (p.Asp1579Asn) rs369751362
NM_002474.3(MYH11):c.4756C>G (p.Gln1586Glu) rs794728680
NM_002474.3(MYH11):c.4770G>A (p.Lys1590=) rs11648119
NM_002474.3(MYH11):c.4774A>C (p.Arg1592=) rs114556043
NM_002474.3(MYH11):c.4791+16G>T rs189463893
NM_002474.3(MYH11):c.4791+226T>C
NM_002474.3(MYH11):c.4791+4C>T rs142108062
NM_002474.3(MYH11):c.4792-108T>C
NM_002474.3(MYH11):c.4792-6G>C rs766965358
NM_002474.3(MYH11):c.4809G>A (p.Thr1603=) rs140577744
NM_002474.3(MYH11):c.4826G>A (p.Arg1609Gln) rs190316422
NM_002474.3(MYH11):c.4834C>T (p.Arg1612Cys) rs748356212
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln) rs34321232
NM_002474.3(MYH11):c.4872G>A (p.Gly1624=) rs764800035
NM_002474.3(MYH11):c.4884C>T (p.Asp1628=) rs780786328
NM_002474.3(MYH11):c.4899C>T (p.Ala1633=) rs760584464
NM_002474.3(MYH11):c.4953+15G>A rs767255396
NM_002474.3(MYH11):c.4953+18C>T rs371462392
NM_002474.3(MYH11):c.4953+63G>A
NM_002474.3(MYH11):c.4954-14G>C rs375979600
NM_002474.3(MYH11):c.4954-196G>T
NM_002474.3(MYH11):c.4954-63C>T
NM_002474.3(MYH11):c.4993C>T (p.Arg1665Cys) rs768569707
NM_002474.3(MYH11):c.4994G>T (p.Arg1665Leu) rs144813247
NM_002474.3(MYH11):c.5053T>C (p.Leu1685=) rs1057522597
NM_002474.3(MYH11):c.5082+20G>A rs527381094
NM_002474.3(MYH11):c.5083-46C>A
NM_002474.3(MYH11):c.5093C>T (p.Ala1698Val) rs779639232
NM_002474.3(MYH11):c.5094C>T (p.Ala1698=) rs771742318
NM_002474.3(MYH11):c.5157T>C (p.Ser1719=) rs771625605
NM_002474.3(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.3(MYH11):c.5171+86T>G
NM_002474.3(MYH11):c.5172-13G>A rs373378619
NM_002474.3(MYH11):c.5172-14C>T rs34839877
NM_002474.3(MYH11):c.5172-255G>A
NM_002474.3(MYH11):c.5172-286C>G
NM_002474.3(MYH11):c.5172-5C>T rs574893374
NM_002474.3(MYH11):c.5214C>T (p.Ile1738=) rs1439627120
NM_002474.3(MYH11):c.5215G>A (p.Ala1739Thr) rs1029371842
NM_002474.3(MYH11):c.5226G>C (p.Glu1742Asp) rs144421849
NM_002474.3(MYH11):c.5247G>A (p.Gln1749=) rs757501817
NM_002474.3(MYH11):c.5261C>T (p.Ala1754Val) rs904032269
NM_002474.3(MYH11):c.5269G>A (p.Asp1757Asn) rs752996609
NM_002474.3(MYH11):c.5273G>A (p.Arg1758Gln) rs142546324
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile) rs138059405
NM_002474.3(MYH11):c.5277C>T (p.Val1759=) rs112564682
NM_002474.3(MYH11):c.5295+76C>T
NM_002474.3(MYH11):c.5296-49C>G
NM_002474.3(MYH11):c.5296-4C>T rs183176702
NM_002474.3(MYH11):c.5313C>T (p.Asn1771=) rs190675029
NM_002474.3(MYH11):c.5328G>A (p.Glu1776=) rs773366562
NM_002474.3(MYH11):c.5336C>T (p.Thr1779Met) rs201960644
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=) rs35295469
NM_002474.3(MYH11):c.5375G>A (p.Arg1792Gln) rs751495086
NM_002474.3(MYH11):c.5379G>A (p.Gln1793=) rs375230260
NM_002474.3(MYH11):c.5393G>A (p.Arg1798Gln) rs148938946
NM_002474.3(MYH11):c.5411T>C (p.Met1804Thr) rs1085307503
NM_002474.3(MYH11):c.5422G>A (p.Val1808Ile) rs780870767
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=) rs1050162
NM_002474.3(MYH11):c.5450C>T (p.Ala1817Val) rs142654744
NM_002474.3(MYH11):c.5451G>A (p.Ala1817=) rs774717188
NM_002474.3(MYH11):c.5454G>A (p.Ala1818=) rs374486989
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr) rs147710374
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=) rs1050163
NM_002474.3(MYH11):c.5485C>G (p.Gln1829Glu) rs1005977032
NM_002474.3(MYH11):c.5490C>A (p.Val1830=)
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.3(MYH11):c.5504+115C>G
NM_002474.3(MYH11):c.5504+268C>G
NM_002474.3(MYH11):c.5504+6C>A rs371348553
NM_002474.3(MYH11):c.5504+8G>C rs148691719
NM_002474.3(MYH11):c.5516C>T (p.Ala1839Val) rs112948385
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=) rs28505375
NM_002474.3(MYH11):c.5528C>T (p.Ser1843Leu) rs148621523
NM_002474.3(MYH11):c.5566C>T (p.Leu1856=) rs142639688
NM_002474.3(MYH11):c.5573T>G (p.Val1858Gly) rs794728670
NM_002474.3(MYH11):c.5581G>A (p.Glu1861Lys) rs139418145
NM_002474.3(MYH11):c.5585G>A (p.Arg1862His) rs146228576
NM_002474.3(MYH11):c.5586C>G (p.Arg1862=) rs542765381
NM_002474.3(MYH11):c.5595C>T (p.Ala1865=) rs760286479
NM_002474.3(MYH11):c.5614-18del rs1555550026
NM_002474.3(MYH11):c.5635G>A (p.Val1879Ile) rs138206921
NM_002474.3(MYH11):c.5666C>T (p.Ala1889Val) rs369950711
NM_002474.3(MYH11):c.5676G>C (p.Glu1892Asp) rs113964173
NM_002474.3(MYH11):c.5691C>T (p.Asn1897=) rs149566621
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser) rs79129097
NM_002474.3(MYH11):c.5732C>A (p.Thr1911Lys) rs748516947
NM_002474.3(MYH11):c.5755C>T (p.Arg1919Cys) rs750085824
NM_002474.3(MYH11):c.5757C>T (p.Arg1919=) rs138168272
NM_002474.3(MYH11):c.5760G>A (p.Glu1920=) rs199997929
NM_002474.3(MYH11):c.5767G>A (p.Ala1923Thr) rs571504063
NM_002474.3(MYH11):c.5767G>T (p.Ala1923Ser) rs571504063
NM_002474.3(MYH11):c.5786+12G>A rs748529228
NM_002474.3(MYH11):c.5786+18C>T rs769309834
NM_002474.3(MYH11):c.5786+220C>A
NM_002474.3(MYH11):c.5786+6_5786+8del rs1064794454
NM_002474.3(MYH11):c.5787-230C>A
NM_002474.3(MYH11):c.5787-4661C>T rs373484327
NM_002474.3(MYH11):c.5787-4672G>A
NM_002474.3(MYH11):c.5787-4705C>A rs765457680
NM_002474.3(MYH11):c.5787-4707C>A rs111588143
NM_002474.3(MYH11):c.5787-4707C>G rs111588143
NM_002474.3(MYH11):c.5787-4708C>G rs200884440
NM_002474.3(MYH11):c.5787-4709C>A rs1057524493
NM_002474.3(MYH11):c.5787-4714dup rs747392139
NM_002474.3(MYH11):c.5787-4733CT[2] rs747642850
NM_002474.3(MYH11):c.5787-4737G>A rs769187225
NM_002474.3(MYH11):c.5787-4966C>A
NM_002474.3(MYH11):c.5787-4998A>G
NM_002474.3(MYH11):c.5788C>T (p.Arg1930Ter) rs772670393
NM_002474.3(MYH11):c.5796C>T (p.Asn1932=) rs149529195
NM_002474.3(MYH11):c.5800A>T (p.Thr1934Ser) rs113667224
NM_002474.3(MYH11):c.5829A>G (p.Gly1943=) rs199752132
NM_002474.3(MYH11):c.5873C>T (p.Thr1958Met) rs149701021
NM_002474.3(MYH11):c.5887G>A (p.Ala1963Thr) rs146413415

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.