Gene entry
CCNF
cyclin F
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 3
CCNF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “cyclin F”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs200324356Conflicting interpretationssingle nucleotide variantDevelopmental and epileptic encephalopathy, 1|Seizure|Autosomal recessive nonsyndromic hearing loss 86|Caused by mutation in the TBC1 domain family, member 24|Developmental and epileptic encephalopathy, 1|Autosomal dominant nonsyndromic hearing loss 65|Familial infantile myoclonic epilepsy
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.