R11G (p.Arg11Gly) variant of RAMP1 (O60894)
R11G (p.Arg11Gly) in RAMP1 (O60894) 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.
R11G (p.Arg11Gly) variant details
- p.Arg11Gly
- gnomAD 2-237859706-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- REVEL 0.03
- CADD 20.10
- PolyPhen-2 0.06
- SIFT 0.24
- Population evidence available
- Structural context available
- Literature evidence available