D15G (p.Asp15Gly) variant of ETFB (P38117)
D15G (p.Asp15Gly) in ETFB (P38117) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data and structural context.
D15G (p.Asp15Gly) variant details
- p.Asp15Gly
- TOPMed rs981006954
- gnomAD rs981006954
- Missense
- Variant Prioritization Score for Impact Estimate 0.789
- REVEL 0.87
- CADD 32.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available