T11I (p.Thr11Ile) variant of IKBKB (O14920)
T11I (p.Thr11Ile) in IKBKB (O14920) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Severe combined immunodeficiency due to IKK2 deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
T11I (p.Thr11Ile) variant details
- p.Thr11Ile
- rs1388981077
- ClinGen CA371088276
- ClinVar RCV001967241
- gnomAD rs1388981077
- Uncertain significance
- Severe combined immunodeficiency due to IKK2 deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.305
- REVEL 0.13
- CADD 22.40
- PolyPhen-2 0.01
- SIFT 0.15
- ClinVar: Uncertain significance (Severe combined immunodeficiency due to IKK2 deficiency)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available