P9Q (p.Pro9Gln) variant of RAMP1 (O60894)
P9Q (p.Pro9Gln) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
P9Q (p.Pro9Gln) variant details
- p.Pro9Gln
- gnomAD 2-237859701-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.253
- REVEL 0.02
- CADD 6.71
- PolyPhen-2 0.00
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available