Figure 1.
Spectrum of 38 unique TNFRSF13B variants identified in 161 PAD patients, showing the exonic locations, affected protein domains, AlphaMissense pathogenicity heatmap, population allele frequency, and CADD predicted damaging score compared with MSC and other variants observed in normal populations based on Genome Aggregation Database (gnomAD).

Spectrum of 38 unique TNFRSF13B variants identified in 161 PAD patients, showing the exonic locations, affected protein domains, AlphaMissense pathogenicity heatmap, population allele frequency, and CADD predicted damaging score compared with MSC and other variants observed in normal populations based on Genome Aggregation Database (gnomAD).

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