NM_004086.3(COCH):c.1055C>G (p.Thr352Ser) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002054369.5
Allele description [Variation Report for NM_004086.3(COCH):c.1055C>G (p.Thr352Ser)]
NM_004086.3(COCH):c.1055C>G (p.Thr352Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024