P98T (p.Pro98Thr) variant of CNGA1 (P29973)
P98T (p.Pro98Thr) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
P98T (p.Pro98Thr) variant details
- p.Pro98Thr
- Ensembl rs79647861
- Missense
- Variant Prioritization Score for Impact Estimate 0.225
- REVEL 0.04
- CADD 19.90
- PolyPhen-2 0.06
- SIFT 0.07
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available