R61G (p.Arg61Gly) variant of RAMP1 (O60894)
R61G (p.Arg61Gly) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
R61G (p.Arg61Gly) variant details
- p.Arg61Gly
- gnomAD 2-237877352-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.151
- REVEL 0.04
- CADD 22.70
- PolyPhen-2 0.05
- SIFT 0.04
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available