P9A (p.Pro9Ala) variant of RAMP1 (O60894)
P9A (p.Pro9Ala) 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, published literature, and structural context.
P9A (p.Pro9Ala) variant details
- p.Pro9Ala
- gnomAD 2-237859700-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.137
- REVEL 0.09
- CADD 8.00
- PolyPhen-2 0.01
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available