V6G (p.Val6Gly) variant of ABCG2 (Q9UNQ0)
V6G (p.Val6Gly) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
V6G (p.Val6Gly) variant details
- p.Val6Gly
- gnomAD rs1388119295
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.34
- CADD 4.75
- PolyPhen-2 0.03
- SIFT 0.22
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available