ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign by Center for Human Genetics, Inc

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Total variants: 17
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NM_002474.3(MYH11):c.3859-14C>T rs763714252
NM_002474.3(MYH11):c.3874G>A (p.Val1292Ile) rs151058774
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3963+6T>C rs373371913
NM_002474.3(MYH11):c.4240G>A (p.Ala1414Thr) rs112467954
NM_002474.3(MYH11):c.4506C>T (p.Leu1502=) rs76890940
NM_002474.3(MYH11):c.4579-14C>T rs377410503
NM_002474.3(MYH11):c.4598C>G (p.Ser1533Cys)
NM_002474.3(MYH11):c.4604G>A (p.Arg1535Gln) rs137934837
NM_002474.3(MYH11):c.4791+4C>T rs142108062
NM_002474.3(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.3(MYH11):c.5450C>T (p.Ala1817Val) rs142654744
NM_002474.3(MYH11):c.5516C>T (p.Ala1839Val) rs112948385
NM_002474.3(MYH11):c.5566C>T (p.Leu1856=) rs142639688
NM_002474.3(MYH11):c.5635G>A (p.Val1879Ile) rs138206921
NM_002474.3(MYH11):c.5787-4733CT[2] rs747642850
NM_002474.3(MYH11):c.5800A>T (p.Thr1934Ser) rs113667224

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