A91T (p.Ala91Thr) variant of XRCC3 (DNA repair protein XRCC3)
A91T (p.Ala91Thr) in XRCC3 (DNA repair protein XRCC3) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
A91T (p.Ala91Thr) variant details
- p.Ala91Thr
- TOPMed rs1032911157
- gnomAD rs1032911157
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.0324
- REVEL 0.01
- CADD 0.06
- PolyPhen-2 0.05
- SIFT 0.51
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Most common in the East Asian population (allele frequency 5.6e-05)
- Structural context available