P9S (p.Pro9Ser) variant of RAMP1 (O60894)
P9S (p.Pro9Ser) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
P9S (p.Pro9Ser) variant details
- p.Pro9Ser
- TOPMed rs1207955479
- gnomAD rs1207955479
- Missense
- Variant Prioritization Score for Impact Estimate 0.122
- REVEL 0.05
- CADD 10.50
- PolyPhen-2 0.02
- SIFT 0.20
- Most common in the Latino/Admixed American population (allele frequency 0.00033)
- Structural context available