T26N (p.Thr26Asn) variant of PRKAA2 (P54646)
T26N (p.Thr26Asn) in PRKAA2 (P54646) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
T26N (p.Thr26Asn) variant details
- p.Thr26Asn
- TOPMed rs1236124861
- gnomAD rs1236124861
- Missense
- Variant Prioritization Score for Impact Estimate 0.356
- REVEL 0.22
- MetaLR 0.10
- MetaSVM -1.06
- CADD 25.10
- PolyPhen-2 0.93
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available