V13V (p.Val13Val) variant of KIT (P10721)
V13V (p.Val13Val) in KIT (P10721) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
V13V (p.Val13Val) variant details
- p.Val13Val
- gnomAD 4-54658053-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.512
- CADD 13.90
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available
- Literature evidence available