T16A (p.Thr16Ala) variant of TGFB2 (P61812)
T16A (p.Thr16Ala) 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 and structural context.
T16A (p.Thr16Ala) variant details
- p.Thr16Ala
- gnomAD rs1423446403
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- REVEL 0.12
- CADD 16.30
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available