NM_015335.5(MED13L):c.5058G>A (p.Thr1686=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000865717.6
Allele description [Variation Report for NM_015335.5(MED13L):c.5058G>A (p.Thr1686=)]
NM_015335.5(MED13L):c.5058G>A (p.Thr1686=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024