A13G (p.Ala13Gly) variant of ARID1B (Q8NFD5)
A13G (p.Ala13Gly) 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.
A13G (p.Ala13Gly) variant details
- p.Ala13Gly
- gnomAD rs1002797837
- Missense
- Variant Prioritization Score for Impact Estimate 0.705
- CADD 15.60
- PolyPhen-2 0.00
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available