M109I (p.Met109Ile) variant of SLC2A2 (P11168)
M109I (p.Met109Ile) 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 0.54 / 1. The record also includes population frequency data and structural context.
M109I (p.Met109Ile) variant details
- p.Met109Ile
- NCI-TCGA Cosmic COSV1000
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.54
- REVEL 0.40
- CADD 22.00
- PolyPhen-2 0.31
- SIFT 0.10
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available