ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign for not provided

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Total variants: 22
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HGVS dbSNP
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3930G>A (p.Val1310=) rs369184213
NM_002474.3(MYH11):c.4206G>A (p.Glu1402=) rs1567699651
NM_002474.3(MYH11):c.4293C>T (p.Asp1431=) rs143588920
NM_002474.3(MYH11):c.4296G>A (p.Leu1432=)
NM_002474.3(MYH11):c.4366-131T>C
NM_002474.3(MYH11):c.4579-140T>C
NM_002474.3(MYH11):c.4579-29T>C
NM_002474.3(MYH11):c.4604G>A (p.Arg1535Gln) rs137934837
NM_002474.3(MYH11):c.5171+86T>G
NM_002474.3(MYH11):c.5172-255G>A
NM_002474.3(MYH11):c.5172-286C>G
NM_002474.3(MYH11):c.5277C>T (p.Val1759=) rs112564682
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+268C>G
NM_002474.3(MYH11):c.5614-8C>T rs376174444
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser) rs79129097
NM_002474.3(MYH11):c.5786+220C>A
NM_002474.3(MYH11):c.5787-4672G>A
NM_002474.3(MYH11):c.5787-4708C>G rs200884440
NM_002474.3(MYH11):c.5787-4998A>G

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