S36G (p.Ser36Gly) variant of CNGA1 (P29973)
S36G (p.Ser36Gly) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
S36G (p.Ser36Gly) variant details
- p.Ser36Gly
- gnomAD rs1212211403
- Missense
- Variant Prioritization Score for Impact Estimate 0.342
- REVEL 0.11
- CADD 27.90
- PolyPhen-2 0.93
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available