F27V (p.Phe27Val) variant of SLC18A2 (Q05940)
F27V (p.Phe27Val) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
F27V (p.Phe27Val) variant details
- p.Phe27Val
- ExAC rs753922210
- gnomAD rs753922210
- Missense
- Variant Prioritization Score for Impact Estimate 0.61
- CADD 25.70
- PolyPhen-2 0.28
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available