N26S (p.Asn26Ser) variant of MYD88 (Q99836)
N26S (p.Asn26Ser) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
N26S (p.Asn26Ser) variant details
- p.Asn26Ser
- TOPMed rs1700990813
- Missense
- Variant Prioritization Score for Impact Estimate 0.609
- CADD 23.70
- PolyPhen-2 0.95
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available