NM_004130.4(GYG1):c.137C>G (p.Ser46Cys) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 5, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000426412.1
Allele description [Variation Report for NM_004130.4(GYG1):c.137C>G (p.Ser46Cys)]
NM_004130.4(GYG1):c.137C>G (p.Ser46Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024