A50D (p.Ala50Asp) variant of RAMP1 (O60894)
A50D (p.Ala50Asp) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
A50D (p.Ala50Asp) variant details
- p.Ala50Asp
- gnomAD rs1273933225
- Missense
- Variant Prioritization Score for Impact Estimate 0.241
- REVEL 0.11
- CADD 15.40
- PolyPhen-2 0.33
- SIFT 0.13
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available