P13P (p.Pro13Pro) variant of MYD88 (Q99836)
P13P (p.Pro13Pro) in MYD88 (Q99836) is a synonymous 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.
P13P (p.Pro13Pro) variant details
- p.Pro13Pro
- rs1292597861
- gnomAD 3-38138739-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.161
- AlphaMissense 0.28
- MetaLR 0.03
- MetaSVM -1.15
- CADD 3.41
- PolyPhen-2 0.98
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available