Format

Send to

Choose Destination
Genet Res (Camb). 2019 Jun 13;101:e8. doi: 10.1017/S0016672319000065.

In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.

Author information

1
Department of Pediatrics,The University of Iowa,Iowa City,IA,USA.
2
Medical Scientist Training Program,University of Iowa,Iowa City,IA,USA.
3
Omics Laboratory,Department of Ophthalmology,Byers Eye Institute,Stanford University,Palo Alto,CA,USA.
4
Department of Anthropology,The University of Iowa,Iowa City,IA,USA.

Abstract

Compound heterozygotes occur when different variants at the same locus on both maternal and paternal chromosomes produce a recessive trait. Here we present the tool VarCount for the quantification of variants at the individual level. We used VarCount to characterize compound heterozygous coding variants in patients with epileptic encephalopathy and in the 1000 Genomes Project participants. The Epi4k data contains variants identified by whole exome sequencing in patients with either Lennox-Gastaut Syndrome (LGS) or infantile spasms (IS), as well as their parents. We queried the Epi4k dataset (264 trios) and the phased 1000 Genomes Project data (2504 participants) for recessive variants. To assess enrichment, transcript counts were compared between the Epi4k and 1000 Genomes Project participants using minor allele frequency (MAF) cutoffs of 0.5 and 1.0%, and including all ancestries or only probands of European ancestry. In the Epi4k participants, we found enrichment for rare, compound heterozygous variants in six genes, including three involved in neuronal growth and development - PRTG (p = 0.00086, 1% MAF, combined ancestries), TNC (p = 0.022, 1% MAF, combined ancestries) and MACF1 (p = 0.0245, 0.5% MAF, EU ancestry). Due to the total number of transcripts considered in these analyses, the enrichment detected was not significant after correction for multiple testing and higher powered or prospective studies are necessary to validate the candidacy of these genes. However, PRTG, TNC and MACF1 are potential novel recessive epilepsy genes and our results highlight that compound heterozygous variants should be considered in sporadic epilepsy.

KEYWORDS:

bioinformatics; compound heterozygous; epilepsy; genetics

PMID:
31190668
DOI:
10.1017/S0016672319000065

Supplemental Content

Full text links

Icon for Cambridge University Press
Loading ...
Support Center