Q79P (p.Gln79Pro) variant of TGFB2 (P61812)
Q79P (p.Gln79Pro) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data, published literature, and structural context.
Q79P (p.Gln79Pro) variant details
- p.Gln79Pro
- gnomAD 1-218346937-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.466
- REVEL 0.33
- CADD 28.70
- PolyPhen-2 0.43
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available