Letter | Published:

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

Nature volume 493, pages 216220 (10 January 2013) | Download Citation

  • A Corrigendum to this article was published on 13 March 2013


Establishing the age of each mutation segregating in contemporary human populations is important to fully understand our evolutionary history1,2 and will help to facilitate the development of new approaches for disease-gene discovery3. Large-scale surveys of human genetic variation have reported signatures of recent explosive population growth4,5,6, notable for an excess of rare genetic variants, suggesting that many mutations arose recently. To more quantitatively assess the distribution of mutation ages, we resequenced 15,336 genes in 6,515 individuals of European American and African American ancestry and inferred the age of 1,146,401 autosomal single nucleotide variants (SNVs). We estimate that approximately 73% of all protein-coding SNVs and approximately 86% of SNVs predicted to be deleterious arose in the past 5,000–10,000 years. The average age of deleterious SNVs varied significantly across molecular pathways, and disease genes contained a significantly higher proportion of recently arisen deleterious SNVs than other genes. Furthermore, European Americans had an excess of deleterious variants in essential and Mendelian disease genes compared to African Americans, consistent with weaker purifying selection due to the Out-of-Africa dispersal. Our results better delimit the historical details of human protein-coding variation, show the profound effect of recent human history on the burden of deleterious SNVs segregating in contemporary populations, and provide important practical information that can be used to prioritize variants in disease-gene discovery.

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Data deposits

Filtered sets of annotated variants and their allele frequencies are available at (http://evs.gs.washington.edu/EVS/) and genotypes and phenotypes from a large subset of individuals are also available through dbGaP (http://www.ncbi.nlm.nih.gov/gap) using the following accession information: NHLBI GO-ESP: Women’s Health Initiative Exome Sequencing Project (WHI) – WHISP, WHISP_Subject_Phenotypes, pht002246.v2.p2, phs000281.v2.p2; NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (JHS), ESP_HeartGO_JHS_LDLandEOMI_Subject_Phenotypes, pht002539.v1.p1, phs000402.v1.p1; NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (FHS), HeartGO_FHS_LDLandEOMI_PhenotypeDataFile, pht002476.v1.p1, phs000401.v1.p1; NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (CHS), HeartGO_CHS_LDL_PhenotypeDataFile, pht002536.v1.p1, phs000400.v1.p1; NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (ARIC), ESP_ARIC_LDLandEOMI_Sample, pht002466.v1.p1, phs000398.v1.p1;NHLBIGO-ESP: Lung Cohorts Exome Sequencing Project (Cystic Fibrosis), ESP_LungGO_CF_PA_Culture_Data, pht002227.v1.p1, phs000254.v1.p1; NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI), ESP_Broad_EOMI_Subject_Phenotypes, pht001437.v1.p1, phs000279.v1.p1; NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Pulmonary Arterial Hypertension), PAH_Subject_Phenotypes_Baseline_Measures, pht002277.v1.p1, phs000290.v1.p1; NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Lung Health Study of Chronic Obstructive Pulmonary Disease), LHS_COPD_Subject_Phenotypes_Baseline_Measures, pht002272.v1.p1, phs000291.v1.p1.


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We acknowledge the support of the National Heart, Lung and Blood Institute (NHLBI), the contributions of the research institutions that participated in this study, the study investigators, field staff and study participants who created this resource for biomedical research, and the Population Genetics Project Team of the NHLBI. We thank J. Wilson and R. Do for critical feedback on the manuscript. Funding for the GO (Grand Opportunity) Exome Sequencing Project was provided by NHLBI grants RC2 HL-103010 (Heart GO), RC2 HL-102923 (Lung GO) and RC2 HL-102924 (WHISP). The exome sequencing was was supported by NHLBI grants RC2 HL-102925 (Broad GO) and RC2 HL-102926 (Seattle GO).

Author information


  1. Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA

    • Wenqing Fu
    • , Timothy D. O’Connor
    • , Mark J. Rieder
    • , Jay Shendure
    • , Deborah A. Nickerson
    • , Michael J. Bamshad
    •  & Joshua M. Akey
  2. Department of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, USA

    • Goo Jun
    • , Hyun Min Kang
    •  & Goncalo Abecasis
  3. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA

    • Suzanne M. Leal
  4. Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA

    • Stacey Gabriel
    •  & David Altshuler
  5. Department of Pediatrics, University of Washington, Seattle, Washington 98195, USA

    • Michael J. Bamshad
  6. *Lists of participants and affiliations appear in the Supplementary Information

    • NHLBI Exome Sequencing Project


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W.F. and J.M.A. conceived the analyses. D.A.N., S.G., M.J.R. and D.A. oversaw data generation and quality control. G.J., H.M.K. and G.A. developed algorithms and identified SNVs from the sequencing data. W.F. carried out the majority of analyses with contributions from T.D.O. W.F., M.J.B., J.S. and J.M.A. analysed the data and wrote the manuscript with contributions from all authors. W.F., T.D.O., S.M.L., J.S., M.J.R., D.A.N., M.J.B. and J.M.A. are members of the Seattle Grand Opportunity (GO) group and G.J., H.M.K., G.A., S.G. and D.A. are members of the Broad GO group, which are both sub-groups of the NHLBI Exome Sequencing Project (ESP).

Competing interests

The authors declare no competing financial interests.

Corresponding authors

Correspondence to Wenqing Fu or Joshua M. Akey.

Supplementary information

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  1. 1.

    Supplementary Information

    This file contains Supplementary Text and Data, Supplementary References, Supplementary Tables 1-4 and Supplementary Figures 1-15 (see Table of Contents for more details).

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