P26Q (p.Pro26Gln) variant of KCNJ5 (P48544)
P26Q (p.Pro26Gln) in KCNJ5 (P48544) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
P26Q (p.Pro26Gln) variant details
- p.Pro26Gln
- TOPMed rs1237737451
- gnomAD rs1237737451
- Missense
- Variant Prioritization Score for Impact Estimate 0.614
- REVEL 0.57
- MetaLR 0.85
- MetaSVM 0.13
- CADD 23.90
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available