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A map of constrained coding regions in the human genome.

Abstract：

:Deep catalogs of genetic variation from thousands of humans enable the detection of intraspecies constraint by identifying coding regions with a scarcity of variation. While existing techniques summarize constraint for entire genes, single gene-wide metrics conceal regional constraint variability within each gene. Therefore, we have created a detailed map of constrained coding regions (CCRs) by leveraging variation observed among 123,136 humans from the Genome Aggregation Database. The most constrained CCRs are enriched for pathogenic variants in ClinVar and mutations underlying developmental disorders. CCRs highlight protein domain families under high constraint and suggest unannotated or incomplete protein domains. The highest-percentile CCRs complement existing variant prioritization methods when evaluating de novo mutations in studies of autosomal dominant disease. Finally, we identify highly constrained CCRs within genes lacking known disease associations. This observation suggests that CCRs may identify regions under strong purifying selection that, when mutated, cause severe developmental phenotypes or embryonic lethality.

journal_name

Nat Genet

journal_title

Nature genetics

authors

Havrilla JM,Pedersen BS,Layer RM,Quinlan AR

doi

10.1038/s41588-018-0294-6

subject

Has Abstract

pub_date

2019-01-01 00:00:00

pages

88-95

issue

1

eissn

1061-4036

issn

1546-1718

pii

10.1038/s41588-018-0294-6

journal_volume

51

pub_type

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