F38S (p.Phe38Ser) variant of CNGA1 (P29973)
F38S (p.Phe38Ser) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
F38S (p.Phe38Ser) variant details
- p.Phe38Ser
- ExAC rs777692611
- gnomAD rs777692611
- Missense
- Variant Prioritization Score for Impact Estimate 0.223
- REVEL 0.14
- CADD 19.30
- PolyPhen-2 0.01
- SIFT 0.40
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available