NM_032581.4(HYCC1):c.991+13T>C AND Hypomyelination and Congenital Cataract
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002092623.5
Allele description [Variation Report for NM_032581.4(HYCC1):c.991+13T>C]
NM_032581.4(HYCC1):c.991+13T>C
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024