ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 79 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001128228.3(TPRN):c.770C>T (p.Pro257Leu) rs745997859 0.00009
NM_001128228.3(TPRN):c.691C>T (p.Arg231Trp) rs886044045 0.00004
NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys) rs370001536 0.00003

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