NM_001378964.1(CDON):c.2139T>C (p.Asp713=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 24, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000877995.3
Allele description
NM_001378964.1(CDON):c.2139T>C (p.Asp713=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 7, 2023