S7R (p.Ser7Arg) variant of TGFB2 (P61812)
S7R (p.Ser7Arg) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
S7R (p.Ser7Arg) variant details
- p.Ser7Arg
- TOPMed rs1558219899
- Missense
- Variant Prioritization Score for Impact Estimate 0.218
- REVEL 0.14
- CADD 17.10
- PolyPhen-2 0.01
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available