S34P (p.Ser34Pro) variant of MYD88 (Q99836)
S34P (p.Ser34Pro) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
S34P (p.Ser34Pro) variant details
- p.Ser34Pro
- gnomAD 3-38138800-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- CADD 24.60
- PolyPhen-2 0.70
- SIFT 0.12
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available
- Literature evidence available