N96S (p.Asn96Ser) variant of LHCGR (P22888)
N96S (p.Asn96Ser) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
N96S (p.Asn96Ser) variant details
- p.Asn96Ser
- TOPMed rs1668873542
- Missense
- Variant Prioritization Score for Impact Estimate 0.221
- REVEL 0.30
- CADD 6.50
- PolyPhen-2 0.01
- SIFT 0.49
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available