S20G (p.Ser20Gly) variant of TGFB2 (P61812)
S20G (p.Ser20Gly) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S20G (p.Ser20Gly) variant details
- p.Ser20Gly
- gnomAD 1-218346759-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.151
- REVEL 0.03
- CADD 21.40
- PolyPhen-2 0.01
- SIFT 0.64
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available