NM_005121.3(MED13):c.5266T>G (p.Cys1756Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003887391.6
Allele description [Variation Report for NM_005121.3(MED13):c.5266T>G (p.Cys1756Gly)]
NM_005121.3(MED13):c.5266T>G (p.Cys1756Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024