N26N (p.Asn26Asn) variant of MYD88 (Q99836)
N26N (p.Asn26Asn) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
N26N (p.Asn26Asn) variant details
- p.Asn26Asn
- rs1423428080
- gnomAD 3-38138778-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.241
- CADD 12.70
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available
- Literature evidence available