Q37K (p.Gln37Lys) variant of SLC2A4 (P14672)
Q37K (p.Gln37Lys) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data, published literature, and structural context.
Q37K (p.Gln37Lys) variant details
- p.Gln37Lys
- gnomAD 17-7283320-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.74
- REVEL 0.71
- CADD 24.80
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available