AutismKB 2.0

Variant Details for C12orf49


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Basic Information Top
Gene Symbol:C12orf49 ( FLJ21415 )
Gene Full Name: chromosome 12 open reading frame 49
Band: 12q24.22
Quick LinksEntrez ID:79794; OMIM: NA; Uniprot ID:CL049_HUMAN; ENSEMBL ID: ENSG00000111412; HGNC ID: 26128
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 5 0 0 1 0 0 6
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000102 12 12q12-24.33 46092533 132022120 85929587 gain external link Szatmari, 2007
AutCNV0000146 12 12q24.21-24.33 115707280 133777650 18070370 gain external link Marshall, 2008
AutCNV0004447 12 12q24.22-24.23 116883864 118394874 1511010 gain external link Nord, 2011
AutCNV0004303 12 12q24.21-q24.33 115685617 133779461 18093844 gain external link Sanders, 2011
AutCNV0005842 12 12q24.22 115655372 115797029 141657 gain external link Egger G, 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
No related data!
NGS Other Mutations Top
Chr Pos Ref Alt Coding AA Validated iFish Prediction iFish Probability Reference
12 117175608 C T Y Cukier HN, 2014
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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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