NM_012243.3(SLC35A3):c.69A>T (p.Thr23=) AND Autism spectrum disorder - epilepsy - arthrogryposis syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003583778.1
Allele description [Variation Report for NM_012243.3(SLC35A3):c.69A>T (p.Thr23=)]
NM_012243.3(SLC35A3):c.69A>T (p.Thr23=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024