A49T (p.Ala49Thr) variant of LHCGR (P22888)
A49T (p.Ala49Thr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
A49T (p.Ala49Thr) variant details
- p.Ala49Thr
- Ensembl rs1670167773
- Missense
- Variant Prioritization Score for Impact Estimate 0.244
- REVEL 0.05
- CADD 9.82
- PolyPhen-2 0.14
- SIFT 0.46
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available