NM_004064.5(CDKN1B):c.349C>T (p.Pro117Ser) AND not provided
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- Jun 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000585589.25
Allele description [Variation Report for NM_004064.5(CDKN1B):c.349C>T (p.Pro117Ser)]
NM_004064.5(CDKN1B):c.349C>T (p.Pro117Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024