Somatic Mutation–Lifespan Relationship
Explore how annual somatic mutation rates in clonally derived intestinal crypts scale inversely with lifespan across mammals, then inspect the underlying migrated SNP and INDEL catalogue.
Lower annual mutation rates accompany longer lifespans
The study-level relationship is the primary result. Each point below is a species summary; it is not a SNP-level association and does not establish that an individual variant causes longevity.
The line and confidence band are an exploratory OLS visualization calculated from the displayed species summaries. The evidence cards report the paper's allometric-model results.
Choose a mammalian WGS dataset
Choose one of 16 clonal intestinal-crypt WGS catalogues. Historical SPEED labels and RDS identifiers are retained as provenance; these are neither single-cell transcriptomic genotypes nor germline GWAS datasets.
Human records
Filters are applied on the server to the complete migrated text files. A maximum of 100 rows is returned per request; every source column remains available in each row's expandable details.
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Primary study and source datasets
The displayed catalogue is linked to a comparative mammalian somatic-mutation study of 208 intestinal crypts from 56 individuals across 16 species.