NM_015046.7(SETX):c.4612C>T (p.Arg1538Trp) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000644810.9
Allele description [Variation Report for NM_015046.7(SETX):c.4612C>T (p.Arg1538Trp)]
NM_015046.7(SETX):c.4612C>T (p.Arg1538Trp)
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024