G13D (p.Gly13Asp) variant of RARA (Retinoic acid receptor alpha)
G13D (p.Gly13Asp) in RARA (Retinoic acid receptor alpha) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
G13D (p.Gly13Asp) variant details
- p.Gly13Asp
- ExAC rs761512575
- gnomAD rs761512575
- Missense
- Variant Prioritization Score for Impact Estimate 0.408
- REVEL 0.27
- CADD 19.00
- PolyPhen-2 0.01
- SIFT 0.21
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available