N38N (p.Asn38Asn) variant of MYD88 (Q99836)
N38N (p.Asn38Asn) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
N38N (p.Asn38Asn) variant details
- p.Asn38Asn
- rs867343970
- gnomAD 3-38138814-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.151
- CADD 10.00
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available
- Literature evidence available