R7P (p.Arg7Pro) variant of RAMP1 (O60894)
R7P (p.Arg7Pro) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
R7P (p.Arg7Pro) variant details
- p.Arg7Pro
- gnomAD 2-237859695-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.142
- REVEL 0.06
- CADD 13.70
- PolyPhen-2 0.16
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available