ClinVar Miner

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

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Total variants: 57
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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.3895G>A (p.Ala1299Thr) rs1388360113
NM_002474.3(MYH11):c.3932C>T (p.Ala1311Val) rs185720909
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.4078C>G (p.Gln1360Glu) rs1555553235
NM_002474.3(MYH11):c.4177G>C (p.Gly1393Arg) rs143620567
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.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.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.4538T>A (p.Met1513Lys) rs794728669
NM_002474.3(MYH11):c.4561G>A (p.Asp1521Asn) rs794728679
NM_002474.3(MYH11):c.4578+5G>C rs1555552121
NM_002474.3(MYH11):c.4603C>T (p.Arg1535Trp) rs143402648
NM_002474.3(MYH11):c.4632G>C (p.Met1544Ile) rs1064797005
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.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.4993C>T (p.Arg1665Cys) rs768569707
NM_002474.3(MYH11):c.4994G>T (p.Arg1665Leu) rs144813247
NM_002474.3(MYH11):c.5093C>T (p.Ala1698Val) rs779639232
NM_002474.3(MYH11):c.5215G>A (p.Ala1739Thr) rs1029371842
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.5375G>A (p.Arg1792Gln) rs751495086
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.5450C>T (p.Ala1817Val) rs142654744
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr) rs147710374
NM_002474.3(MYH11):c.5485C>G (p.Gln1829Glu) rs1005977032
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.3(MYH11):c.5516C>T (p.Ala1839Val) rs112948385
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.5635G>A (p.Val1879Ile) rs138206921
NM_002474.3(MYH11):c.5666C>T (p.Ala1889Val) rs369950711
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.5767G>A (p.Ala1923Thr) rs571504063
NM_002474.3(MYH11):c.5767G>T (p.Ala1923Ser) rs571504063
NM_002474.3(MYH11):c.5787-4705C>A rs765457680
NM_002474.3(MYH11):c.5788C>T (p.Arg1930Ter) rs772670393
NM_002474.3(MYH11):c.5887G>A (p.Ala1963Thr) rs146413415

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