N41D (p.Asn41Asp) variant of ABCG2 (Q9UNQ0)
N41D (p.Asn41Asp) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
N41D (p.Asn41Asp) variant details
- p.Asn41Asp
- Ensembl rs746161650
- Missense
- Variant Prioritization Score for Impact Estimate 0.404
- REVEL 0.26
- CADD 19.10
- PolyPhen-2 0.05
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available