p.Glu66dup variant of TGFB2 (P61812)
p.Glu66dup in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data, published literature, and structural context.
p.Glu66dup variant details
- rs1656702122
- gnomAD 1-218346895-C-CGG
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.627
- CADD 20.60
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available