P37P (p.Pro37Pro) variant of SPTBN4 (Q9H254)
P37P (p.Pro37Pro) in SPTBN4 (Q9H254) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
P37P (p.Pro37Pro) variant details
- p.Pro37Pro
- rs1055113527
- gnomAD 19-40472732-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0814
- CADD 0.10
- Most common in the Non-Finnish European population (allele frequency 3.2e-05)
- Structural context available
- Literature evidence available