P78Q (p.Pro78Gln) variant of SLC22A2 (O15244)
P78Q (p.Pro78Gln) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
P78Q (p.Pro78Gln) variant details
- p.Pro78Gln
- gnomAD rs1270581848
- Missense
- Variant Prioritization Score for Impact Estimate 0.0744
- REVEL 0.05
- CADD 4.44
- PolyPhen-2 0.22
- SIFT 0.59
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available