E38G (p.Glu38Gly) variant of TGFB2 (P61812)
E38G (p.Glu38Gly) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data, published literature, and structural context.
E38G (p.Glu38Gly) variant details
- p.Glu38Gly
- gnomAD 1-218346814-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.73
- REVEL 0.76
- CADD 32.00
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available