NM_144672.4(OTOA):c.96G>T (p.Leu32Phe) AND Autosomal recessive nonsyndromic hearing loss 22
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000764036.2
Allele description [Variation Report for NM_144672.4(OTOA):c.96G>T (p.Leu32Phe)]
NM_144672.4(OTOA):c.96G>T (p.Leu32Phe)
Condition(s)
-
BioSample links for Nucleotide (Select 1353698081) (1)
BioSample
-
Microbe sample from Streptococcus suis
Microbe sample from Streptococcus suisbiosample
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See more...Assertion and evidence details
Last Updated: May 1, 2024