NM_030973.4(MED25):c.1727C>G (p.Ala576Gly) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Apr 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002057053.20
Allele description [Variation Report for NM_030973.4(MED25):c.1727C>G (p.Ala576Gly)]
NM_030973.4(MED25):c.1727C>G (p.Ala576Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024