NM_015335.5(MED13L):c.2997-27C>T AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 7, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001673308.2
Allele description [Variation Report for NM_015335.5(MED13L):c.2997-27C>T]
NM_015335.5(MED13L):c.2997-27C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023