NM_003106.4(SOX2):c.243T>G (p.Leu81=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 19, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000614482.8
Allele description [Variation Report for NM_003106.4(SOX2):c.243T>G (p.Leu81=)]
NM_003106.4(SOX2):c.243T>G (p.Leu81=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024