T26T (p.Thr26Thr) variant of TGFB2 (P61812)
T26T (p.Thr26Thr) in TGFB2 (P61812) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
T26T (p.Thr26Thr) variant details
- p.Thr26Thr
- rs755643964
- gnomAD 1-218346779-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.253
- CADD 13.80
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available