D47G (p.Asp47Gly) variant of RAMP1 (O60894)
D47G (p.Asp47Gly) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
D47G (p.Asp47Gly) variant details
- p.Asp47Gly
- gnomAD 2-237877311-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.19
- REVEL 0.08
- CADD 23.00
- PolyPhen-2 0.73
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available
- Literature evidence available