NM_000455.5(STK11):c.129C>G (p.Ala43=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000679316.5
Allele description [Variation Report for NM_000455.5(STK11):c.129C>G (p.Ala43=)]
NM_000455.5(STK11):c.129C>G (p.Ala43=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024