R10Q (p.Arg10Gln) variant of RAMP1 (O60894)
R10Q (p.Arg10Gln) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
R10Q (p.Arg10Gln) variant details
- p.Arg10Gln
- TOPMed rs1287976125
- Missense
- Variant Prioritization Score for Impact Estimate 0.267
- REVEL 0.02
- CADD 19.40
- PolyPhen-2 0.00
- SIFT 0.19
- Most common in the REMAINING population (allele frequency 1.8e-05)
- Structural context available