P156Q (p.Pro156Gln) variant of ARNT (P27540)
P156Q (p.Pro156Gln) in ARNT (P27540) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data.
P156Q (p.Pro156Gln) variant details
- p.Pro156Gln
- rs778405288
- ExAC rs778405288
- gnomAD rs778405288
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.6
- REVEL 0.45
- CADD 28.20
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 3.3e-05)