ClinVar Miner

List of variants in gene MYO3A reported as likely benign for auditory system disease

Included ClinVar conditions (549):
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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_017433.5(MYO3A):c.*246C>T rs12261671
NM_017433.5(MYO3A):c.-132A>G rs7073224
NM_017433.5(MYO3A):c.-189C>G rs188597967
NM_017433.5(MYO3A):c.1743G>A (p.Glu581=) rs41279908
NM_017433.5(MYO3A):c.2497G>T (p.Ala833Ser) rs33947968
NM_017433.5(MYO3A):c.3589G>A (p.Glu1197Lys) rs75801377
NM_017433.5(MYO3A):c.4335A>G (p.Lys1445=) rs34615182
NM_017433.5(MYO3A):c.4462A>G (p.Lys1488Glu) rs34204285
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile) rs33968748
NM_017433.5(MYO3A):c.624C>T (p.Asp208=) rs35010955
NM_017433.5(MYO3A):c.660C>T (p.Ala220=) rs34067308

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