G7S (p.Gly7Ser) variant of MYD88 (Q99836)
G7S (p.Gly7Ser) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
G7S (p.Gly7Ser) variant details
- p.Gly7Ser
- gnomAD 3-38138719-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0762
- CADD 0.64
- PolyPhen-2 0.00
- SIFT 0.77
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available