A57T (p.Ala57Thr) variant of LHCGR (P22888)
A57T (p.Ala57Thr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A57T (p.Ala57Thr) variant details
- p.Ala57Thr
- cosmic curated COSV10882
- 1000Genomes rs576351203
- ExAC rs576351203
- Missense
- Variant Prioritization Score for Impact Estimate 0.169
- REVEL 0.04
- CADD 17.10
- Most common in the 1KG:CDX population (allele frequency 0.0057)
- Structural context available