P6S (p.Pro6Ser) variant of MYD88 (Q99836)
P6S (p.Pro6Ser) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
P6S (p.Pro6Ser) variant details
- p.Pro6Ser
- cosmic curated COSV57182
- TOPMed rs1300885784
- gnomAD rs1300885784
- Missense
- Variant Prioritization Score for Impact Estimate 0.27
- CADD 5.50
- PolyPhen-2 0.00
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available