A24S (p.Ala24Ser) variant of LHCGR (P22888)
A24S (p.Ala24Ser) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
A24S (p.Ala24Ser) variant details
- p.Ala24Ser
- gnomAD rs1223955730
- Missense
- Variant Prioritization Score for Impact Estimate 0.128
- REVEL 0.08
- CADD 4.56
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available