R7G (p.Arg7Gly) variant of RAMP1 (O60894)
R7G (p.Arg7Gly) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
R7G (p.Arg7Gly) variant details
- p.Arg7Gly
- gnomAD 2-237859694-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.163
- REVEL 0.02
- CADD 7.40
- PolyPhen-2 0.00
- SIFT 0.61
- Most common in the East Asian population (allele frequency 3.2e-05)
- Structural context available
- Literature evidence available