P38T (p.Pro38Thr) variant of LHCGR (P22888)
P38T (p.Pro38Thr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
P38T (p.Pro38Thr) variant details
- p.Pro38Thr
- TOPMed rs1412890389
- Missense
- Variant Prioritization Score for Impact Estimate 0.256
- REVEL 0.13
- CADD 19.50
- PolyPhen-2 0.09
- SIFT 0.20
- Most common in the South Asian population (allele frequency 1.3e-05)
- Structural context available