N32S (p.Asn32Ser) variant of SLC2A2 (P11168)
N32S (p.Asn32Ser) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
N32S (p.Asn32Ser) variant details
- p.Asn32Ser
- ExAC rs775531825
- TOPMed rs775531825
- gnomAD rs775531825
- Missense
- Variant Prioritization Score for Impact Estimate 0.608
- REVEL 0.59
- CADD 25.80
- PolyPhen-2 0.98
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 9.7e-05)
- Structural context available