V39V (p.Val39Val) variant of SLC18A2 (Q05940)
V39V (p.Val39Val) in SLC18A2 (Q05940) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
V39V (p.Val39Val) variant details
- p.Val39Val
- rs781006451
- gnomAD 10-117241810-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.432
- CADD 11.20
- Most common in the South Asian population (allele frequency 0.00022)
- Structural context available
- Literature evidence available