N16D (p.Asn16Asp) variant of ABCG2 (Q9UNQ0)
N16D (p.Asn16Asp) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
N16D (p.Asn16Asp) variant details
- p.Asn16Asp
- Ensembl rs1560706429
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- REVEL 0.09
- CADD 8.23
- PolyPhen-2 0.01
- SIFT 0.05
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available