Ranking human genes based on their tolerance to functional genetic variation can greatly facilitate patient genome interpretation. It is well established, however, that different parts of proteins can have different functions, suggesting that it will ultimately be more informative to focus attention on functionally distinct portions of genes. Here we evaluate the intolerance of genic sub-regions using two biological sub-region classifications. We show that the intolerance scores of these sub-regions significantly correlate with reported pathogenic mutations. This observation extends the utility of intolerance scores to indicating where pathogenic mutations are mostly likely to fall within genes
A wide variety of functional domains exist within human genes. Since different domains vary in their...
Integration of protein structural information with human genetic variation and pathogenic mutations ...
Loss-of-function variants in innate immunity genes are associated with Mendelian disorders in the fo...
Ranking human genes based on their tolerance to functional genetic variation can greatly facilitate ...
<div><p>A central challenge in interpreting personal genomes is determining which mutations most lik...
All proteomes contain both proteins and polypeptide segments that don't form a defined three-dimensi...
Whole exomes of patients with a genetic disorder are nowadays routinely sequenced but interpretation...
Noncoding sequence contains pathogenic mutations. Yet, compared with mutations in protein-coding seq...
<div><p>The decreasing cost of sequencing is leading to a growing repertoire of personal genomes. Ho...
A wide variety of functional domains exist within human genes. Since different domains vary in their...
peer reviewedMissense variant interpretation is challenging. Essential regions for protein function ...
Integration of protein structural information with human genetic variation and pathogenic mutations ...
There is a longstanding interest in identifying the subset of our genome that is the most essential ...
Increasing evidence indicates that genes containing disease causal variation have distinct functiona...
A text file containing the subset of genes for which we have reported pathogenic variants (3,046 gen...
A wide variety of functional domains exist within human genes. Since different domains vary in their...
Integration of protein structural information with human genetic variation and pathogenic mutations ...
Loss-of-function variants in innate immunity genes are associated with Mendelian disorders in the fo...
Ranking human genes based on their tolerance to functional genetic variation can greatly facilitate ...
<div><p>A central challenge in interpreting personal genomes is determining which mutations most lik...
All proteomes contain both proteins and polypeptide segments that don't form a defined three-dimensi...
Whole exomes of patients with a genetic disorder are nowadays routinely sequenced but interpretation...
Noncoding sequence contains pathogenic mutations. Yet, compared with mutations in protein-coding seq...
<div><p>The decreasing cost of sequencing is leading to a growing repertoire of personal genomes. Ho...
A wide variety of functional domains exist within human genes. Since different domains vary in their...
peer reviewedMissense variant interpretation is challenging. Essential regions for protein function ...
Integration of protein structural information with human genetic variation and pathogenic mutations ...
There is a longstanding interest in identifying the subset of our genome that is the most essential ...
Increasing evidence indicates that genes containing disease causal variation have distinct functiona...
A text file containing the subset of genes for which we have reported pathogenic variants (3,046 gen...
A wide variety of functional domains exist within human genes. Since different domains vary in their...
Integration of protein structural information with human genetic variation and pathogenic mutations ...
Loss-of-function variants in innate immunity genes are associated with Mendelian disorders in the fo...