NM_000751.3(CHRND):c.414C>T (p.Phe138=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001704263.15
Allele description [Variation Report for NM_000751.3(CHRND):c.414C>T (p.Phe138=)]
NM_000751.3(CHRND):c.414C>T (p.Phe138=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024