NM_000388.4(CASR):c.732C>T (p.Ser244=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002181369.6
Allele description [Variation Report for NM_000388.4(CASR):c.732C>T (p.Ser244=)]
NM_000388.4(CASR):c.732C>T (p.Ser244=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024