P98Q (p.Pro98Gln) variant of CNGA1 (P29973)
P98Q (p.Pro98Gln) in CNGA1 (P29973) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
P98Q (p.Pro98Gln) variant details
- p.Pro98Gln
- TOPMed rs1023306743
- gnomAD rs1023306743
- Missense
- Variant Prioritization Score for Impact Estimate 0.204
- REVEL 0.04
- CADD 19.60
- PolyPhen-2 0.00
- SIFT 0.07
- Most common in the HGDP:BURUSHO population (allele frequency 0.042)
- Structural context available