R3Q (p.Arg3Gln) variant of RAMP1 (O60894)
R3Q (p.Arg3Gln) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data, published literature, and structural context.
R3Q (p.Arg3Gln) variant details
- p.Arg3Gln
- gnomAD 2-237859683-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0707
- REVEL 0.04
- CADD 6.24
- PolyPhen-2 0.14
- SIFT 0.44
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available