NM_000455.5(STK11):c.168G>C (p.Gly56=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000424839.1
Allele description [Variation Report for NM_000455.5(STK11):c.168G>C (p.Gly56=)]
NM_000455.5(STK11):c.168G>C (p.Gly56=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024