N26H (p.Asn26His) variant of MYD88 (Q99836)
N26H (p.Asn26His) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data, published literature, and structural context.
N26H (p.Asn26His) variant details
- p.Asn26His
- gnomAD 3-38138776-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.629
- CADD 26.30
- PolyPhen-2 0.99
- SIFT 0.03
- Most common in the HGDP:MBUTI population (allele frequency 0.083)
- Structural context available
- Literature evidence available