NM_174889.4(NDUFAF2):c.-97A>G AND Cockayne syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000337453.14
Allele description [Variation Report for NM_174889.4(NDUFAF2):c.-97A>G]
NM_174889.4(NDUFAF2):c.-97A>G
Condition(s)
- Name:
- Cockayne syndrome
- Synonyms:
- Cockayne's syndrome; Dwarfism-retinal atrophy-deafness syndrome; Progeria-like syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0016006; MedGen: C0009207
Assertion and evidence details
Last Updated: Oct 8, 2024