AutismKB 2.0

Variant Details for C12orf35


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Basic Information Top
Gene Symbol:C12orf35 ( FLJ10652,FLJ20696 )
Gene Full Name: chromosome 12 open reading frame 35
Band: 12p11.21
Quick LinksEntrez ID:55196; OMIM: NA; Uniprot ID:CL035_HUMAN; ENSEMBL ID: ENSG00000174718; HGNC ID:
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 3 1 0 0 0 0 4
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000364 12 12p11.21 30708733 33308733 2600000 external link Zwaag, 2009
AutCNV0001416 12 12p11.21 32034552 32140098 105546 gain external link Pinto, 2010
AutCNV0000708 12 12p11.1-12.1 24295351 34760977 10465626 loss external link Soysal, 2011
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
12 32134096 T C Sanger sequencing De Rubeis S, 2014
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
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!




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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