NM_001378609.3(OTOGL):c.2270T>C (p.Phe757Ser) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jul 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002623630.4
Allele description [Variation Report for NM_001378609.3(OTOGL):c.2270T>C (p.Phe757Ser)]
NM_001378609.3(OTOGL):c.2270T>C (p.Phe757Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024