NM_003334.4(UBA1):c.206G>A (p.Arg69Gln) AND Infantile-onset X-linked spinal muscular atrophy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000872075.8
Allele description
NM_003334.4(UBA1):c.206G>A (p.Arg69Gln)
Condition(s)
- Name:
- Infantile-onset X-linked spinal muscular atrophy
- Synonyms:
- ARTHROGRYPOSIS, X-LINKED, TYPE I; SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE; Arthrogryposis multiplex congenita, distal, X-linked; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0010532; MedGen: C1844934; Orphanet: 1145; OMIM: 301830
Assertion and evidence details
Last Updated: Feb 28, 2024