F22F (p.Phe22Phe) variant of RAMP1 (O60894)
F22F (p.Phe22Phe) in RAMP1 (O60894) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
F22F (p.Phe22Phe) variant details
- p.Phe22Phe
- rs137909772
- gnomAD 2-237877237-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.228
- CADD 5.61
- Most common in the Finnish in Finland (FIN) population (allele frequency 5.6e-05)
- Structural context available
- Literature evidence available