M29I (p.Met29Ile) variant of HLA-B (P01889)
M29I (p.Met29Ile) in HLA-B (P01889) 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 0.33 / 1. The record also includes population frequency data and structural context.
M29I (p.Met29Ile) variant details
- p.Met29Ile
- NCI-TCGA Cosmic COSV1013
- cosmic curated COSV10131
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.20
- CADD 24.00
- PolyPhen-2 0.08
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.4e-05)
- Structural context available