N75D (p.Asn75Asp) variant of SLC2A2 (P11168)
N75D (p.Asn75Asp) in SLC2A2 (P11168) 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.
N75D (p.Asn75Asp) variant details
- p.Asn75Asp
- gnomAD rs1207297111
- Missense
- Variant Prioritization Score for Impact Estimate 0.197
- REVEL 0.29
- CADD 0.10
- PolyPhen-2 0.00
- SIFT 0.52
- Most common in the South Asian population (allele frequency 9.3e-05)
- Structural context available