D65N (p.Asp65Asn) variant of SLC2A2 (P11168)
D65N (p.Asp65Asn) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
D65N (p.Asp65Asn) variant details
- p.Asp65Asn
- ExAC rs754585542
- gnomAD rs754585542
- Missense
- Variant Prioritization Score for Impact Estimate 0.374
- REVEL 0.23
- CADD 4.17
- PolyPhen-2 0.00
- SIFT 0.40
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available