V26M (p.Val26Met) variant of SLC18A2 (Q05940)
V26M (p.Val26Met) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data, published literature, and structural context.
V26M (p.Val26Met) variant details
- p.Val26Met
- gnomAD 10-117241769-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.817
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available