NM_001077415.3(CRELD1):c.93C>T (p.Pro31=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003434426.4
Allele description [Variation Report for NM_001077415.3(CRELD1):c.93C>T (p.Pro31=)]
NM_001077415.3(CRELD1):c.93C>T (p.Pro31=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024