ClinVar Miner

List of variants in gene combination MYH11, NDE1 studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP
NM_001040113.1(MYH11):c.3721G>A (p.Ala1241Thr) rs16967494
NM_001040113.1(MYH11):c.3918C>T (p.Ala1306=) rs190546350
NM_001040113.1(MYH11):c.3951G>A (p.Val1317=) rs369184213
NM_001040113.1(MYH11):c.3988C>T (p.Leu1330=) rs12907
NM_001040113.1(MYH11):c.3990G>A (p.Leu1330=)
NM_001040113.1(MYH11):c.4339C>T (p.Arg1447Trp) rs766841864
NM_001040113.1(MYH11):c.4424C>T (p.Ala1475Val) rs370240337
NM_001040113.1(MYH11):c.4625G>A (p.Arg1542Gln) rs137934837
NM_001040113.1(MYH11):c.5014C>T (p.Arg1672Cys) rs768569707
NM_001040113.1(MYH11):c.5073C>G (p.Ser1691Arg) rs760908992
NM_001040113.1(MYH11):c.5083G>C (p.Asp1695His) rs1239423939
NM_001040113.1(MYH11):c.5197G>A (p.Ala1733Thr) rs376154041
NM_001040113.1(MYH11):c.5236G>A (p.Ala1746Thr) rs1029371842
NM_001040113.1(MYH11):c.5294G>A (p.Arg1765Gln) rs142546324
NM_001040113.1(MYH11):c.5385G>A (p.Gln1795=) rs1064797209
NM_001040113.1(MYH11):c.5635-8C>T rs376174444
NM_001040113.1(MYH11):c.5717A>G (p.Asn1906Ser) rs79129097
NM_001040113.1(MYH11):c.5808-9_5808-8delCT rs747642850
NM_001040113.1(MYH11):c.5821C>A (p.Gln1941Lys) rs765457680
NM_001040114.1(MYH11):c.4694C>T (p.Thr1565Met) rs111854563
NM_001040114.1(MYH11):c.4856G>A (p.Arg1619His)
NM_001143979.1(NDE1):c.948-10T>G rs775809843
NM_001143979.1(NDE1):c.948-5858G>A rs112564682
NM_001143979.1(NDE1):c.948-6986C>T rs1050162
NM_001143979.1(NDE1):c.948-7025C>T rs1050163
NM_002474.2(MYH11):c.3866T>C (p.Val1289Ala) rs16967510
NM_002474.2(MYH11):c.3874G>A (p.Val1292Ile) rs151058774
NM_002474.2(MYH11):c.3895G>A (p.Ala1299Thr) rs1388360113
NM_002474.2(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.2(MYH11):c.3932C>T (p.Ala1311Val) rs185720909
NM_002474.2(MYH11):c.4016G>A (p.Arg1339His) rs374271463
NM_002474.2(MYH11):c.4078C>G (p.Gln1360Glu) rs1555553235
NM_002474.2(MYH11):c.4158C>T (p.Thr1386=) rs112377790
NM_002474.2(MYH11):c.4240G>A (p.Ala1414Thr) rs112467954
NM_002474.2(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.2(MYH11):c.4293C>T (p.Asp1431=) rs143588920
NM_002474.2(MYH11):c.4303G>A (p.Asp1435Asn) rs794728668
NM_002474.2(MYH11):c.4319G>A (p.Arg1440Gln) rs763467593
NM_002474.2(MYH11):c.4418G>T (p.Arg1473Ile) rs758663266
NM_002474.2(MYH11):c.4459_4464delTCCCTG (p.Ser1487_Leu1488del) rs1555552158
NM_002474.2(MYH11):c.4506C>T (p.Leu1502=) rs76890940
NM_002474.2(MYH11):c.4522A>G (p.Met1508Val) rs35176378
NM_002474.2(MYH11):c.4538T>A (p.Met1513Lys) rs794728669
NM_002474.2(MYH11):c.4561G>A (p.Asp1521Asn) rs794728679
NM_002474.2(MYH11):c.4578+1G>A rs397514037
NM_002474.2(MYH11):c.4603C>T (p.Arg1535Trp) rs143402648
NM_002474.2(MYH11):c.4717A>G (p.Lys1573Glu) rs151101824
NM_002474.2(MYH11):c.4735G>A (p.Asp1579Asn) rs369751362
NM_002474.2(MYH11):c.4756C>G (p.Gln1586Glu) rs794728680
NM_002474.2(MYH11):c.4826G>A (p.Arg1609Gln) rs190316422
NM_002474.2(MYH11):c.4834C>T (p.Arg1612Cys) rs748356212
NM_002474.2(MYH11):c.4861A>C (p.Lys1621Gln) rs34321232
NM_002474.2(MYH11):c.4994G>T (p.Arg1665Leu) rs144813247
NM_002474.2(MYH11):c.5093C>T (p.Ala1698Val) rs779639232
NM_002474.2(MYH11):c.5269G>A (p.Asp1757Asn) rs752996609
NM_002474.2(MYH11):c.5275G>A (p.Val1759Ile) rs138059405
NM_002474.2(MYH11):c.5375G>A (p.Arg1792Gln) rs751495086
NM_002474.2(MYH11):c.5393G>A (p.Arg1798Gln) rs148938946
NM_002474.2(MYH11):c.5411T>C (p.Met1804Thr) rs1085307503
NM_002474.2(MYH11):c.5422G>A (p.Val1808Ile) rs780870767
NM_002474.2(MYH11):c.5450C>T (p.Ala1817Val) rs142654744
NM_002474.2(MYH11):c.5485C>G (p.Gln1829Glu) rs1005977032
NM_002474.2(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.2(MYH11):c.5516C>T (p.Ala1839Val) rs112948385
NM_002474.2(MYH11):c.5517G>A (p.Ala1839=) rs28505375
NM_002474.2(MYH11):c.5529G>A (p.Ser1843=) rs146024732
NM_002474.2(MYH11):c.5573T>G (p.Val1858Gly) rs794728670
NM_002474.2(MYH11):c.5581G>A (p.Glu1861Lys) rs139418145
NM_002474.2(MYH11):c.5585G>A (p.Arg1862His) rs146228576
NM_002474.2(MYH11):c.5635G>A (p.Val1879Ile) rs138206921
NM_002474.2(MYH11):c.5666C>T (p.Ala1889Val) rs369950711
NM_002474.2(MYH11):c.5676G>C (p.Glu1892Asp) rs113964173
NM_002474.2(MYH11):c.5691C>T (p.Asn1897=) rs149566621
NM_002474.2(MYH11):c.5732C>A (p.Thr1911Lys) rs748516947
NM_002474.2(MYH11):c.5755C>T (p.Arg1919Cys) rs750085824
NM_002474.2(MYH11):c.5767G>A (p.Ala1923Thr) rs571504063
NM_002474.2(MYH11):c.5767G>T (p.Ala1923Ser) rs571504063
NM_002474.2(MYH11):c.5787-4707C>T rs111588143
NM_002474.2(MYH11):c.5787-4713C>A rs765030635
NM_002474.2(MYH11):c.5887G>A (p.Ala1963Thr) rs146413415
NM_002474.3(MYH11):c.4206G>A (p.Glu1402=)
NM_002474.3(MYH11):c.4578+2dup rs794728677
NM_002474.3(MYH11):c.4632G>C (p.Met1544Ile) rs1064797005
NM_002474.3(MYH11):c.5441C>T (p.Ser1814Phe) rs759033733
NM_002474.3(MYH11):c.5838_5839del (p.Arg1946Serfs)

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.