V13V (p.Val13Val) variant of VHL (P40337)
V13V (p.Val13Val) in VHL (P40337) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
V13V (p.Val13Val) variant details
- p.Val13Val
- rs996469746
- gnomAD 3-10141886-A-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0918
- CADD 1.57
- Most common in the Non-Finnish European population (allele frequency 5.8e-05)
- Structural context available
- Literature evidence available