P38P (p.Pro38Pro) variant of ARID2 (Q68CP9)
P38P (p.Pro38Pro) in ARID2 (Q68CP9) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
P38P (p.Pro38Pro) variant details
- p.Pro38Pro
- rs1177962366
- gnomAD 12-45730065-T-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.251
- CADD 12.90
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available