NM_015335.5(MED13L):c.3435C>T (p.Val1145=) AND MED13L-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004536214.1
Allele description [Variation Report for NM_015335.5(MED13L):c.3435C>T (p.Val1145=)]
NM_015335.5(MED13L):c.3435C>T (p.Val1145=)
Condition(s)
- Name:
- MED13L-related disorder
- Synonyms:
- MED13L-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 1, 2024