NM_000388.4(CASR):c.1235C>T (p.Thr412Met) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000795003.7
Allele description [Variation Report for NM_000388.4(CASR):c.1235C>T (p.Thr412Met)]
NM_000388.4(CASR):c.1235C>T (p.Thr412Met)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024