M27I (p.Met27Ile) variant of MYD88 (Q99836)
M27I (p.Met27Ile) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
M27I (p.Met27Ile) variant details
- p.Met27Ile
- gnomAD 3-38138781-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- CADD 19.40
- PolyPhen-2 0.00
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available