Overview

Variant ID 29574
Entrez Gene ID 1778
Gene DYNC1H1 (GeneCards)
Location hg19 14:102510723-102510723
hg38 14:102044386-102044386
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000014.8:g.102510723 A>T (Genome Assembly: hg19)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 107349540

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0697
CADD Raw score (version 1.3) 3.392513 (Deleterious)
FATHMM raw prediction score 0.97786 (Tolerated)
SIFT score 0.047 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 1.845 (Tolerated)
PROVEAN score -4.03 (Deleterious)
MetaSVM score -1.121 (Tolerated)
MetaLR score 0.033 (Tolerated)
MCAP score 0.013 (Tolerated)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.37
PhyloP score based on multiple alignment of 100 vertebrates 4.977
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 15.383
Deleterious probability by iFish2 0.0913 (Neutral)
Deleterious probability by DeFine 0.9745 (Deleterious)
Entrez Gene ID 1778 (NCBI Gene)
Official Gene Symbol DYNC1H1 (GeneCards)
Number of variants in DYNC1H1 in this database 6 (view all the variants)
Full name dynein cytoplasmic 1 heavy chain 1
Band 14q32.31
Other IDs Vega: OTTHUMG00000171644
OMIM: 600112
HGNC: HGNC:2961
Ensembl: ENSG00000197102
Other names p22, DHC1, DNCL, DYHC, HL-3, CMT2O, DHC1a, DNCH1, DNECL, Dnchc1, SMALED1
Summary Dyneins are a group of microtubule-activated ATPases that function as molecular motors. They are divided into two subgroups of axonemal and cytoplasmic dyneins. The cytoplasmic dyneins function in intracellular motility, including retrograde axonal transport, protein sorting, organelle movement, and spindle dynamics. Molecules of conventional cytoplasmic dynein are comprised of 2 heavy chain polypeptides and a number of intermediate and light chains.This gene encodes a member of the cytoplasmic dynein heavy chain family. [provided by RefSeq, Oct 2008]

Individual #1

Individual ID 28714951.250 (view all the variants in this individual)
Pubmed ID 28714951
Whose mosaic mutation Patient  
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28714951

Pubmed ID 28714951
Title Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
Journal Nat Neurosci
Publication date 2017.07
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 376;