N7N (p.Asn7Asn) variant of PIM1 (P11309)
N7N (p.Asn7Asn) in PIM1 (P11309) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
N7N (p.Asn7Asn) variant details
- p.Asn7Asn
- rs756412850
- gnomAD 6-37170596-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.556
- CADD 14.20
- Most common in the Latino/Admixed American population (allele frequency 0.00013)
- Structural context available
- Literature evidence available