ClinVar Miner

List of variants in gene MYO15A reported by National Institute on Deafness and Communication Disorders, National Institutes of Health

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.4888C>T (p.Arg1630Cys) rs138861831 0.00280
NM_016239.4(MYO15A):c.3196G>C (p.Ala1066Pro) rs199537186 0.00073
NM_016239.4(MYO15A):c.5777G>A (p.Arg1926His) rs199734245 0.00013
NM_016239.4(MYO15A):c.6302T>C (p.Leu2101Pro) rs201908493 0.00008
NM_016239.4(MYO15A):c.3505C>T (p.Arg1169Ter) rs781546107 0.00001
NM_016239.4(MYO15A):c.4216G>A (p.Glu1406Lys) rs759810756 0.00001
NM_016239.4(MYO15A):c.7006C>T (p.Gln2336Ter) rs1169954783 0.00001
NM_016239.4(MYO15A):c.10572dup (p.Ser3525fs) rs1057519607
NM_016239.4(MYO15A):c.3932T>C (p.Ile1311Thr) rs1057519603
NM_016239.4(MYO15A):c.4528C>T (p.Gln1510Ter) rs779077039
NM_016239.4(MYO15A):c.4570C>T (p.Gln1524Ter) rs1209665716
NM_016239.4(MYO15A):c.5005C>T (p.Gln1669Ter) rs1567641234
NM_016239.4(MYO15A):c.6178-2A>G rs878854415
NM_016239.4(MYO15A):c.6589C>T (p.Gln2197Ter) rs779445819
NM_016239.4(MYO15A):c.6944del (p.Gly2315fs) rs1057519604
NM_016239.4(MYO15A):c.8224+3A>G rs1057519605
NM_016239.4(MYO15A):c.9229+2T>C rs1057519606

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