ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 8 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_001256317.3(TMPRSS3):c.413C>A (p.Ala138Glu) rs147231991 0.00146
NM_001256317.3(TMPRSS3):c.1273G>A (p.Ala425Thr) rs56264519 0.00105
NM_001256317.3(TMPRSS3):c.325C>T (p.Arg109Trp) rs201632198 0.00010
NM_001256317.3(TMPRSS3):c.346G>A (p.Val116Met) rs200090033 0.00004
NM_001256317.3(TMPRSS3):c.646C>T (p.Arg216Cys) rs145913750 0.00002
NM_001256317.3(TMPRSS3):c.208del (p.His70fs) rs727503493

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