AutismKB 2.0

Variant Details for CHD1L


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Basic Information Top
Gene Symbol:CHD1L ( ALC1,CHDL,FLJ22530 )
Gene Full Name: chromodomain helicase DNA binding protein 1-like
Band: 1q21.1
Quick LinksEntrez ID:9557; OMIM: 613039; Uniprot ID:CHD1L_HUMAN; ENSEMBL ID: ENSG00000131778; HGNC ID: 1916
Relate to Another Database: SFARIGene; denovo-db
Variant Statistic Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
Genetic Category CNVs/SVs de novo Mutations Mosaics SNVs NGS Other Mutations Low-Scale Gene Mutations Linkage Regions Total
Number 10 0 1 0 0 0 11
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000051 1 1q21.1 146555184 147254184 699000 gain external link Szatmari, 2007
AutCNV0000032 1 1q21.1 146555184 147779088 1223904 gain external link Szatmari, 2007
AutCNV0000401 1 1q21-22 145958564 148219890 2261326 gain external link Gregory, 2009
AutCNV0000782 1 1q21.1 146127237 147841663 1714426 gain external link Pinto, 2010
AutCNV0004193 1 1q21.1 146547095 147826658 1279563 loss external link Sanders, 2011
AutCNV0004192 1 1q21.1 146126818 147858208 1731390 gain external link Sanders, 2011
AutCNV0004191 1 1q21.1 145900678 147858944 1958266 gain external link Sanders, 2011
AutCNV0003124 1 1q21.1 146503841 147826658 1322817 gain external link Gai, 2011
AutCNV0003123 1 1q21.1 146501348 147826658 1325310 gain external link Gai, 2011
AutCNV0004681 17 17p13.3;p13.2 2455643 3449869 994226 gain external link Gazzellone MJ, 2014
NGS de novo Mutations Top
iFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
Chr Pos Ref Alt Coding AA Validated Method iFish Prediction iFish Probability Reference
No related data!
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
1 146728216 C T Mosaic Krupp DR, 2017
NGS Other Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
No related data!
Low-Scale Gene Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
No related data!
Linkage Regions Top
Linkage Name Band Chr Marker LOD NPL P Value Reference
No related data!




Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018