NM_173598.6(KSR2):c.2632C>T (p.Pro878Ser) AND KSR2-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003927226.1
Allele description
NM_173598.6(KSR2):c.2632C>T (p.Pro878Ser)
Condition(s)
- Name:
- KSR2-related disorder
- Synonyms:
- KSR2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Aug 11, 2024