R10W (p.Arg10Trp) variant of RAMP1 (O60894)
R10W (p.Arg10Trp) 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 and structural context.
R10W (p.Arg10Trp) variant details
- p.Arg10Trp
- TOPMed rs1486839130
- gnomAD rs1486839130
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.01
- CADD 17.80
- PolyPhen-2 0.00
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 0.0001)
- Structural context available