N26N (p.Asn26Asn) variant of CSRP3 (P50461)
N26N (p.Asn26Asn) in CSRP3 (P50461) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
N26N (p.Asn26Asn) variant details
- p.Asn26Asn
- gnomAD 11-19192371-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.117
- CADD 5.19
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available