R7H (p.Arg7His) variant of RAMP1 (O60894)
R7H (p.Arg7His) 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 and structural context.
R7H (p.Arg7His) variant details
- p.Arg7His
- TOPMed rs2062113128
- Missense
- Variant Prioritization Score for Impact Estimate 0.157
- REVEL 0.10
- CADD 10.40
- PolyPhen-2 0.28
- SIFT 0.55
- Most common in the Latino/Admixed American population (allele frequency 3.2e-05)
- Structural context available