NM_014423.4(AFF4):c.2482C>T (p.His828Tyr) AND Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003589623.2
Allele description [Variation Report for NM_014423.4(AFF4):c.2482C>T (p.His828Tyr)]
NM_014423.4(AFF4):c.2482C>T (p.His828Tyr)
Condition(s)
- Name:
- Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome
- Synonyms:
- COGNITIVE IMPAIRMENT, COARSE FACIES, HEART DEFECTS, OBESITY, PULMONARY INVOLVEMENT, SHORT STATURE, AND SKELETAL DYSPLASIA; Chops syndrome
- Identifiers:
- MONDO: MONDO:0014609; MedGen: C4085597; Orphanet: 444077; OMIM: 616368
Assertion and evidence details
Last Updated: Sep 29, 2024