N92T (p.Asn92Thr) variant of LHCGR (P22888)
N92T (p.Asn92Thr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
N92T (p.Asn92Thr) variant details
- p.Asn92Thr
- ExAC rs762692771
- gnomAD rs762692771
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.23
- CADD 19.60
- PolyPhen-2 0.26
- SIFT 0.20
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available