C6S (p.Cys6Ser) variant of RAMP1 (O60894)
C6S (p.Cys6Ser) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
C6S (p.Cys6Ser) variant details
- p.Cys6Ser
- gnomAD rs1326475722
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.05
- CADD 10.10
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available