M13V (p.Met13Val) variant of SLC2A1 (P11166)
M13V (p.Met13Val) in SLC2A1 (P11166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
M13V (p.Met13Val) variant details
- p.Met13Val
- ExAC rs774411009
- gnomAD rs774411009
- Missense
- Variant Prioritization Score for Impact Estimate 0.512
- REVEL 0.36
- CADD 14.40
- PolyPhen-2 0.00
- SIFT 1.00
- Population evidence available
- Structural context available