V17V (p.Val17Val) variant of TGFB2 (P61812)
V17V (p.Val17Val) in TGFB2 (P61812) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
V17V (p.Val17Val) variant details
- p.Val17Val
- rs549320294
- gnomAD 1-218346752-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.136
- CADD 7.75
- Most common in the 1KG:ITU population (allele frequency 0.0049)
- Structural context available
- Literature evidence available