N75K (p.Asn75Lys) variant of SLC2A2 (P11168)
N75K (p.Asn75Lys) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
N75K (p.Asn75Lys) variant details
- p.Asn75Lys
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.213
- REVEL 0.32
- CADD 0.77
- PolyPhen-2 0.02
- SIFT 0.50
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available