R37G (p.Arg37Gly) variant of RAMP1 (O60894)
R37G (p.Arg37Gly) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- ExAC rs781748441
- TOPMed rs781748441
- gnomAD rs781748441
- Missense
- Variant Prioritization Score for Impact Estimate 0.177
- REVEL 0.09
- CADD 12.40
- PolyPhen-2 0.08
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available