S36T (p.Ser36Thr) variant of SMARCA2 (P51531)
S36T (p.Ser36Thr) in SMARCA2 (P51531) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, published literature, and structural context.
S36T (p.Ser36Thr) variant details
- p.Ser36Thr
- gnomAD 9-2029128-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.521
- REVEL 0.36
- AlphaMissense 0.39
- MetaLR 0.76
- MetaSVM 0.64
- CADD 27.00
- PolyPhen-2 0.97
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available