V36A (p.Val36Ala) variant of ABCG2 (Q9UNQ0)
V36A (p.Val36Ala) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
V36A (p.Val36Ala) variant details
- p.Val36Ala
- ESP rs146004187
- ExAC rs146004187
- TOPMed rs146004187
- gnomAD rs146004187
- Missense
- Variant Prioritization Score for Impact Estimate 0.444
- REVEL 0.32
- CADD 23.40
- PolyPhen-2 0.51
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available