P19Q (p.Pro19Gln) variant of LHCGR (P22888)
P19Q (p.Pro19Gln) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
P19Q (p.Pro19Gln) variant details
- p.Pro19Gln
- 1000Genomes rs188002889
- Missense
- Variant Prioritization Score for Impact Estimate 0.22
- REVEL 0.24
- CADD 4.10
- PolyPhen-2 0.00
- SIFT 0.32
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available