NM_015046.7(SETX):c.199T>C (p.Leu67=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 14, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001497099.6
Allele description [Variation Report for NM_015046.7(SETX):c.199T>C (p.Leu67=)]
NM_015046.7(SETX):c.199T>C (p.Leu67=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024