Figure 1.
High prevalence of clonal hematopoiesis at low VAF in individuals ≥80 years, dominated by DNMT3A and TET2 variants. (A) Mutational landscape for somatic variants detected in this elderly cohort. Blue and red color indicate respectively 1 or ≥2 variants per gene. (B) Proportion of individuals carrying a somatic variant in recurrently (>10×) mutated genes. (C) VAFs for all detected variants in recurrently (>10×) mutated genes. (D) Bar plot showing the proportion of individuals with CH, stratified into 3 age groups. (E) Forest plot showing the odds ratio with 95% CI for the presence of most prevalent gene variants according to a 1-year increase in age. (F-G) Highest observed VAF (scatter plot) and number of somatic variants (violin plot) per individual categorized in 3 age groups. The horizontal line and rectangle represent median values for the respective group. The category of spliceosome variants includes SF3B1, SRSF2, and U2AF1.

High prevalence of clonal hematopoiesis at low VAF in individuals ≥80 years, dominated by DNMT3A and TET2 variants. (A) Mutational landscape for somatic variants detected in this elderly cohort. Blue and red color indicate respectively 1 or ≥2 variants per gene. (B) Proportion of individuals carrying a somatic variant in recurrently (>10×) mutated genes. (C) VAFs for all detected variants in recurrently (>10×) mutated genes. (D) Bar plot showing the proportion of individuals with CH, stratified into 3 age groups. (E) Forest plot showing the odds ratio with 95% CI for the presence of most prevalent gene variants according to a 1-year increase in age. (F-G) Highest observed VAF (scatter plot) and number of somatic variants (violin plot) per individual categorized in 3 age groups. The horizontal line and rectangle represent median values for the respective group. The category of spliceosome variants includes SF3B1, SRSF2, and U2AF1.

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