V98L (p.Val98Leu) variant of MAOA (P21397)
V98L (p.Val98Leu) in MAOA (P21397) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
V98L (p.Val98Leu) variant details
- p.Val98Leu
- TOPMed rs1465678248
- gnomAD rs1465678248
- Missense
- Variant Prioritization Score for Impact Estimate 0.206
- REVEL 0.10
- MetaLR 0.03
- MetaSVM -1.08
- CADD 21.60
- SIFT 0.26
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00017)
- Structural context available