A18T (p.Ala18Thr) variant of CDKN1B (P46527)
A18T (p.Ala18Thr) in CDKN1B (P46527) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
A18T (p.Ala18Thr) variant details
- p.Ala18Thr
- gnomAD rs1946486987
- Missense
- Variant Prioritization Score for Impact Estimate 0.459
- REVEL 0.41
- CADD 23.30
- PolyPhen-2 0.41
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available