P19L (p.Pro19Leu) variant of LHCGR (P22888)
P19L (p.Pro19Leu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
P19L (p.Pro19Leu) variant details
- p.Pro19Leu
- cosmic curated COSV54303
- 1000Genomes rs188002889
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.28
- CADD 5.01
- PolyPhen-2 0.00
- SIFT 0.64
- Most common in the Non-Finnish European population (allele frequency 2.8e-06)
- Structural context available