NM_001393500.2(TOMT):c.*244C>A AND Autosomal recessive nonsyndromic hearing loss 63
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001110347.13
Allele description [Variation Report for NM_001393500.2(TOMT):c.*244C>A]
NM_001393500.2(TOMT):c.*244C>A
Condition(s)
Assertion and evidence details
Last Updated: Sep 8, 2024