Q3L (p.Gln3Leu) variant of LHCGR (P22888)
Q3L (p.Gln3Leu) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
Q3L (p.Gln3Leu) variant details
- p.Gln3Leu
- gnomAD rs1670180472
- Missense
- Variant Prioritization Score for Impact Estimate 0.106
- REVEL 0.12
- CADD 5.18
- PolyPhen-2 0.00
- SIFT 0.03
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available