R37Q (p.Arg37Gln) variant of RAMP1 (O60894)
R37Q (p.Arg37Gln) 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.
R37Q (p.Arg37Gln) variant details
- p.Arg37Gln
- cosmic curated COSV54537
- 1000Genomes rs142335491
- ESP rs142335491
- ExAC rs142335491
- Missense
- Variant Prioritization Score for Impact Estimate 0.0485
- REVEL 0.02
- CADD 0.85
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the HGDP:MBUTI population (allele frequency 0.083)
- Structural context available