T51N (p.Thr51Asn) variant of TGFB2 (P61812)
T51N (p.Thr51Asn) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
T51N (p.Thr51Asn) variant details
- p.Thr51Asn
- Ensembl rs1656699420
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.06
- CADD 20.70
- PolyPhen-2 0.05
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available