R34P (p.Arg34Pro) variant of TGFB2 (P61812)
R34P (p.Arg34Pro) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
R34P (p.Arg34Pro) variant details
- p.Arg34Pro
- gnomAD 1-218346802-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.579
- REVEL 0.39
- CADD 32.00
- PolyPhen-2 0.95
- SIFT 0.01
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available