NM_005188.4(CBL):c.33C>T (p.Ala11=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 11, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001820182.4
Allele description [Variation Report for NM_005188.4(CBL):c.33C>T (p.Ala11=)]
NM_005188.4(CBL):c.33C>T (p.Ala11=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024