W56R (p.Trp56Arg) variant of RAMP1 (O60894)
W56R (p.Trp56Arg) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
W56R (p.Trp56Arg) variant details
- p.Trp56Arg
- gnomAD 2-237877337-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.463
- REVEL 0.48
- CADD 25.50
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available