P122T (p.Pro122Thr) variant of CNGA1 (P29973)
P122T (p.Pro122Thr) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
P122T (p.Pro122Thr) variant details
- p.Pro122Thr
- Ensembl rs868453867
- Missense
- Variant Prioritization Score for Impact Estimate 0.111
- REVEL 0.03
- CADD 6.82
- PolyPhen-2 0.00
- SIFT 0.10
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available