ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 21 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_005422.4(TECTA):c.2657A>G (p.Asn886Ser) rs146175803 0.00061
NM_005422.4(TECTA):c.3520C>T (p.Arg1174Ter)
NM_005422.4(TECTA):c.5537T>G (p.Ile1846Ser)
NM_005422.4(TECTA):c.6150C>A (p.Tyr2050Ter)

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