L39F (p.Leu39Phe) variant of RAMP1 (O60894)
L39F (p.Leu39Phe) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
L39F (p.Leu39Phe) variant details
- p.Leu39Phe
- gnomAD rs1324705939
- Missense
- Variant Prioritization Score for Impact Estimate 0.0573
- REVEL 0.05
- CADD 0.01
- PolyPhen-2 0.01
- SIFT 0.59
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available