A26V (p.Ala26Val) variant of RAMP1 (O60894)
A26V (p.Ala26Val) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
A26V (p.Ala26Val) variant details
- p.Ala26Val
- gnomAD 2-237877248-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.308
- REVEL 0.12
- CADD 22.60
- PolyPhen-2 0.25
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available