S13N (p.Ser13Asn) variant of CALCA (P06881)
S13N (p.Ser13Asn) in CALCA (P06881) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- gnomAD rs1555026435
- Missense
- Variant Prioritization Score for Impact Estimate 0.271
- REVEL 0.10
- CADD 21.80
- Most common in the East Asian population (allele frequency 0.00019)