H13H (p.His13His) variant of TGFB2 (P61812)
H13H (p.His13His) in TGFB2 (P61812) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data, published literature, and structural context.
H13H (p.His13His) variant details
- p.His13His
- rs1414431711
- gnomAD 1-218346740-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.586
- CADD 13.70
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available