Overview

Variant ID 1391
Entrez Gene ID 26512
Gene INTS6 (GeneCards)
Location hg19 13:51948834-51948834
hg38 13:51374698-51374698
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500 v2
Mutation(HGVS format) NC_000013.10:g.51948834 G>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 597
Amino acid changes in protein R > *
Position in cDNA 1789
Changes in cDNA C > T
mRNA accession NM_001039937.1
mRNA length 6973
Reference length 115169878

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.9218
CADD Raw score (version 1.3) 13.428341 (Deleterious)
FATHMM raw prediction score 0.98705 (Tolerated)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.04
PhyloP score based on multiple alignment of 100 vertebrates 3.996
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 17.732
Deleterious probability by DeFine 0.953 (Deleterious)
Entrez Gene ID 26512 (NCBI Gene)
Official Gene Symbol INTS6 (GeneCards)
Number of variants in INTS6 in this database 4 (view all the variants)
Full name integrator complex subunit 6
Band 13q14.3
Other IDs Vega: OTTHUMG00000016945
OMIM: 604331
HGNC: HGNC:14879
Ensembl: ENSG00000102786
Other names HDB, INT6, DBI-1, DDX26, DICE1, DDX26A, Notchl2
Summary DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. The protein encoded by this gene is a DEAD box protein that is part of a complex that interacts with the C-terminus of RNA polymerase II and is involved in 3' end processing of snRNAs. In addition, this gene is a candidate tumor suppressor and is located in the critical region of loss of heterozygosity (LOH). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2015]

Individual #1

Individual ID 28867142.05 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Female Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;