R16P (p.Arg16Pro) variant of SLC18A2 (Q05940)
R16P (p.Arg16Pro) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
R16P (p.Arg16Pro) variant details
- p.Arg16Pro
- TOPMed rs925216254
- gnomAD rs925216254
- Missense
- Variant Prioritization Score for Impact Estimate 0.634
- CADD 32.00
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available