NM_014918.5(CHSY1):c.37C>T (p.Leu13=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003395067.4
Allele description
NM_014918.5(CHSY1):c.37C>T (p.Leu13=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024