T18M (p.Thr18Met) variant of MALT1 (Q9UDY8)
T18M (p.Thr18Met) in MALT1 (Q9UDY8) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Combined immunodeficiency due to MALT1 deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
T18M (p.Thr18Met) variant details
- p.Thr18Met
- rs1602263180
- ClinGen CA402570659
- ClinVar RCV000807542
- TOPMed rs1602263180
- Uncertain significance
- Combined immunodeficiency due to MALT1 deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.381
- CADD 19.30
- PolyPhen-2 0.02
- SIFT 0.04
- ClinVar: Uncertain significance (Combined immunodeficiency due to MALT1 deficiency)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.1e-06)
- Structural context available