N31D (p.Asn31Asp) variant of RAMP1 (O60894)
N31D (p.Asn31Asp) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
N31D (p.Asn31Asp) variant details
- p.Asn31Asp
- TOPMed rs1393788019
- gnomAD rs1393788019
- Missense
- Variant Prioritization Score for Impact Estimate 0.0478
- REVEL 0.03
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 0.75
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available