L98F (p.Leu98Phe) variant of LHCGR (P22888)
L98F (p.Leu98Phe) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
L98F (p.Leu98Phe) variant details
- p.Leu98Phe
- cosmic curated COSV54300
- 1000Genomes rs535656263
- ExAC rs535656263
- gnomAD rs535656263
- Missense
- Variant Prioritization Score for Impact Estimate 0.286
- REVEL 0.22
- CADD 17.70
- Most common in the 1KG:CDX population (allele frequency 0.0057)
- Structural context available