S66T (p.Ser66Thr) variant of AICDA (Q9GZX7)
S66T (p.Ser66Thr) in AICDA (Q9GZX7) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
S66T (p.Ser66Thr) variant details
- p.Ser66Thr
- gnomAD rs1236265469
- Missense
- Variant Prioritization Score for Impact Estimate 0.288
- REVEL 0.17
- MetaLR 0.13
- MetaSVM -0.98
- CADD 20.20
- PolyPhen-2 0.03
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available