M16I (p.Met16Ile) variant of CUL3 (Cullin-3)
M16I (p.Met16Ile) in CUL3 (Cullin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
M16I (p.Met16Ile) variant details
- p.Met16Ile
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.292
- REVEL 0.06
- CADD 22.10
- PolyPhen-2 0.08
- SIFT 0.15
- UniProt: Variant assessed as somatic; high impact.
- Population evidence available
- Structural context available