p.Thr17 Ser19del variant of MYD88 (Q99836)
p.Thr17 Ser19del in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
p.Thr17 Ser19del variant details
- rs1197233489
- gnomAD 3-38138742-CTCCTC
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.159
- CADD 11.00
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available
- Literature evidence available