F21F (p.Phe21Phe) variant of CLCN5 (P51795)
F21F (p.Phe21Phe) in CLCN5 (P51795) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
F21F (p.Phe21Phe) variant details
- p.Phe21Phe
- gnomAD X-50042362-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.247
- CADD 10.60
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available