R34S (p.Arg34Ser) variant of TGFB2 (P61812)
R34S (p.Arg34Ser) in TGFB2 (P61812) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
R34S (p.Arg34Ser) variant details
- p.Arg34Ser
- cosmic curated COSV10085
- Missense
- Variant Prioritization Score for Impact Estimate 0.449
- REVEL 0.23
- CADD 23.00
- PolyPhen-2 0.30
- SIFT 0.23
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available