Y38C (p.Tyr38Cys) variant of PIM1 (P11309)
Y38C (p.Tyr38Cys) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
Y38C (p.Tyr38Cys) variant details
- p.Tyr38Cys
- 1000Genomes rs761386793
- ExAC rs761386793
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.40
- CADD 29.90
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the 1KG:CHS population (allele frequency 0.0049)
- Structural context available