D13G (p.Asp13Gly) variant of ARNT (P27540)
D13G (p.Asp13Gly) 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 0.35 / 1. The record also includes population frequency data.
D13G (p.Asp13Gly) variant details
- p.Asp13Gly
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10059
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.354
- REVEL 0.14
- CADD 27.10
- PolyPhen-2 0.70
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)