A109T (p.Ala109Thr) variant of CARD9 (Q9H257)
A109T (p.Ala109Thr) in CARD9 (Q9H257) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Predisposition to invasive fungal disease due to CARD9 deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
A109T (p.Ala109Thr) variant details
- p.Ala109Thr
- ExAC rs766469254
- TOPMed rs766469254
- gnomAD rs766469254
- Uncertain significance
- Predisposition to invasive fungal disease due to CARD9 deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.10
- CADD 13.60
- PolyPhen-2 0.01
- SIFT 0.91
- ClinVar: Uncertain significance (Predisposition to invasive fungal disease due to CARD9 deficienc)
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)