Evidence map›Paper›PMID 37214792›Full record

ArticlebioRxiv : the preprint server for biology2023

A deep catalog of protein-coding variation in 985,830 individuals.

Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Manav Kapoor, Chuanyi Zhang, Joshua Backman, Tyler Joseph, Evan Maxwell, George Mitra and 38 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

48 authors.

Kathie Y SunRegeneron Genetics Center, Tarrytown, NY, USA.
Xiaodong BaiRegeneron Genetics Center, Tarrytown, NY, USA.
Siying ChenRegeneron Genetics Center, Tarrytown, NY, USA.
Suying BaoRegeneron Genetics Center, Tarrytown, NY, USA.
Manav KapoorRegeneron Genetics Center, Tarrytown, NY, USA.
Chuanyi ZhangRegeneron Genetics Center, Tarrytown, NY, USA.
Joshua BackmanRegeneron Genetics Center, Tarrytown, NY, USA.
Tyler JosephRegeneron Genetics Center, Tarrytown, NY, USA.
Evan MaxwellRegeneron Genetics Center, Tarrytown, NY, USA.
George MitraRegeneron Genetics Center, Tarrytown, NY, USA.
Alexander GorovitsRegeneron Genetics Center, Tarrytown, NY, USA.
Adam MansfieldRegeneron Genetics Center, Tarrytown, NY, USA.
Boris BoutkovRegeneron Genetics Center, Tarrytown, NY, USA.
Sujit GokhaleRegeneron Genetics Center, Tarrytown, NY, USA.
Lukas HabeggerRegeneron Genetics Center, Tarrytown, NY, USA.
Anthony MarckettaRegeneron Genetics Center, Tarrytown, NY, USA.
Adam LockeRegeneron Genetics Center, Tarrytown, NY, USA.
Michael D KesslerRegeneron Genetics Center, Tarrytown, NY, USA.
Deepika SharmaRegeneron Genetics Center, Tarrytown, NY, USA.
Jeffrey StaplesRegeneron Genetics Center, Tarrytown, NY, USA.
Jonas BovijnRegeneron Genetics Center, Tarrytown, NY, USA.
Sahar GelfmanRegeneron Genetics Center, Tarrytown, NY, USA.
Alessandro Di GioiaRegeneron Genetics Center, Tarrytown, NY, USA.
Veera RajagopalRegeneron Genetics Center, Tarrytown, NY, USA.
Alexander LopezRegeneron Genetics Center, Tarrytown, NY, USA.
Jennifer Rico VarelaRegeneron Genetics Center, Tarrytown, NY, USA.
Jesus AlegreExperimental Research Unit from the Faculty of Medicine (UIME), National Autonomous University of Mexico (UNAM).
Jaime BerumenExperimental Research Unit from the Faculty of Medicine (UIME), National Autonomous University of Mexico (UNAM).
Roberto Tapia-ConyerExperimental Research Unit from the Faculty of Medicine (UIME), National Autonomous University of Mexico (UNAM).
Pablo Kuri-MoralesExperimental Research Unit from the Faculty of Medicine (UIME), National Autonomous University of Mexico (UNAM).
Jason TorresClinical Trial Service Unit & Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Jonathan EmbersonClinical Trial Service Unit & Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Rory CollinsClinical Trial Service Unit & Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Regeneron Genetics Center
RGC-ME Cohort Partners
Michael CantorRegeneron Genetics Center, Tarrytown, NY, USA.
Timothy ThorntonRegeneron Genetics Center, Tarrytown, NY, USA.
Hyun Min KangRegeneron Genetics Center, Tarrytown, NY, USA.
John OvertonRegeneron Genetics Center, Tarrytown, NY, USA.
Alan R ShuldinerRegeneron Genetics Center, Tarrytown, NY, USA.
M Laura CremonaRegeneron Genetics Center, Tarrytown, NY, USA.
Mona NafdeRegeneron Genetics Center, Tarrytown, NY, USA.
Aris BarasRegeneron Genetics Center, Tarrytown, NY, USA.
Goncalo AbecasisRegeneron Genetics Center, Tarrytown, NY, USA.
Jonathan MarchiniRegeneron Genetics Center, Tarrytown, NY, USA.
Jeffrey G ReidRegeneron Genetics Center, Tarrytown, NY, USA.
William SalernoRegeneron Genetics Center, Tarrytown, NY, USA.
Suganthi BalasubramanianRegeneron Genetics Center, Tarrytown, NY, USA.

Funding

Identification of Genes Involved in Major Mood DisordersZIAMH002843 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2025
$24.5M
Genetic Susceptibility and Biomarkers of Platinum-related ToxicitiesR01CA157823 · NCI · UNIVERSITY OF ROCHESTER · PI TRAVIS, LOIS B. · 2012 to 2025
$11.2M
Intramural NIH HHS ZIA MH002843Medical Research Council MC_UU_00017/2NCI NIH HHS R01 CA157823
6 · The paper itself

Abstract

Coding variants that have significant impact on function can provide insights into the biology of a gene but are typically rare in the population. Identifying and ascertaining the frequency of such rare variants requires very large sample sizes. Here, we present the largest catalog of human protein-coding variation to date, derived from exome sequencing of 985,830 individuals of diverse ancestry to serve as a rich resource for studying rare coding variants. Individuals of African, Admixed American, East Asian, Middle Eastern, and South Asian ancestry account for 20% of this Exome dataset. Our catalog of variants includes approximately 10.5 million missense (54% novel) and 1.1 million predicted loss-of-function (pLOF) variants (65% novel, 53% observed only once). We identified individuals with rare homozygous pLOF variants in 4,874 genes, and for 1,838 of these this work is the first to document at least one pLOF homozygote. Additional insights from the RGC-ME dataset include 1) improved estimates of selection against heterozygous loss-of-function and identification of 3,459 genes intolerant to loss-of-function, 83 of which were previously assessed as tolerant to loss-of-function and 1,241 that lack disease annotations; 2) identification of regions depleted of missense variation in 457 genes that are tolerant to loss-of-function; 3) functional interpretation for 10,708 variants of unknown or conflicting significance reported in ClinVar as cryptic splice sites using splicing score thresholds based on empirical variant deleteriousness scores derived from RGC-ME; and 4) an observation that approximately 3% of sequenced individuals carry a clinically actionable genetic variant in the ACMG SF 3.1 list of genes. We make this important resource of coding variation available to the public through a variant allele frequency browser. We anticipate that this report and the RGC-ME dataset will serve as a valuable reference for understanding rare coding variation and help advance precision medicine efforts.

Identifiers

PMID37214792
PMCPMC10197621

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.