NM_015046.7(SETX):c.6122T>C (p.Ile2041Thr) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000792834.5
Allele description [Variation Report for NM_015046.7(SETX):c.6122T>C (p.Ile2041Thr)]
NM_015046.7(SETX):c.6122T>C (p.Ile2041Thr)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024