I68T (p.Ile68Thr) variant of TGFB2 (P61812)
I68T (p.Ile68Thr) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
I68T (p.Ile68Thr) variant details
- p.Ile68Thr
- Ensembl rs1656702547
- Missense
- Variant Prioritization Score for Impact Estimate 0.465
- REVEL 0.36
- CADD 25.60
- PolyPhen-2 0.16
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available