T26A (p.Thr26Ala) variant of TGFB2 (P61812)
T26A (p.Thr26Ala) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
T26A (p.Thr26Ala) variant details
- p.Thr26Ala
- cosmic curated COSV10820
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.20
- CADD 24.00
- PolyPhen-2 0.25
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available