A13T (p.Ala13Thr) variant of ARID1B (Q8NFD5)
A13T (p.Ala13Thr) in ARID1B (Q8NFD5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data and structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- gnomAD rs1211283818
- Missense
- Variant Prioritization Score for Impact Estimate 0.702
- CADD 16.10
- PolyPhen-2 0.00
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available