AutismKB 2.0

Variant Details for RNF213


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Basic Information Top
Gene Symbol:RNF213 ( C17orf27,DKFZp762N1115,FLJ13051,KIAA1554,KIAA1618,MGC46622,MGC9929,NET57 )
Gene Full Name: ring finger protein 213
Band: 17q25.3
Quick LinksEntrez ID:57674; OMIM: NA; Uniprot ID:ALO17_HUMAN; ENSEMBL ID: ENSG00000173821,ENSG00000180843; HGNC ID: 14539
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 1 1 0 1 0 1 4
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0002140 17 17q25.3 78286177 78327745 41568 loss external link Pinto, 2010
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
17 78263533 G A p.Glu337Lys Sangerneutral0.1434 Krumm N, 2015
NGS Mosaic Mutations Top
Chr Position Ref Alt Genotype Validated Method Reference
No related data!
NGS Other Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
chr17 78242045 6kbdup Y Yuen RK, 2015
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
AutLD0000044 17q25.3 17 D17S784 1.67 - - Auranen, 2002




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  (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