V37F (p.Val37Phe) variant of MAOA (P21397)
V37F (p.Val37Phe) in MAOA (P21397) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
V37F (p.Val37Phe) variant details
- p.Val37Phe
- gnomAD X-43683548-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- REVEL 0.36
- MetaLR 0.59
- MetaSVM -0.19
- CADD 13.80
- PolyPhen-2 0.74
- SIFT 0.02
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available