AutismKB 2.0

Variant Details for SYT15


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Basic Information Top
Gene Symbol:SYT15 ( CHR10SYT,sytXV )
Gene Full Name: synaptotagmin XV
Band: 10q11.22
Quick LinksEntrez ID:83849; OMIM: 608081; Uniprot ID:SYT15_HUMAN; ENSEMBL ID: ENSG00000204176; HGNC ID: 17167
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 9 1 0 0 0 1 11
CNVs/SVs Top
CNV ID Chr Band Start End Size Gain/Loss UCSC Browser Reference
AutCNV0000219 10 10q11.22-11.23 46269073 51450788 5181715 gain external link Christian, 2008
AutCNV0000418 10 10q11.21-11.22 46498042 49246405 2748363 gain external link Gregory, 2009
AutCNV0000417 10 10q11.21-11.22 46498042 47792476 1294434 gain external link Gregory, 2009
AutCNV0000416 10 10q11.21-11.22 46498041 47103815 605774 gain external link Gregory, 2009
AutCNV0000415 10 10q11.21-11.22 46029208 48228375 2199167 gain external link Gregory, 2009
AutCNV0000420 10 10q11.21-11.22 46604460 47359747 755287 loss external link Gregory, 2009
AutCNV0000419 10 10q11.21-11.22 46550732 48331399 1780667 gain external link Gregory, 2009
AutCNV0005143 10 10q11.22 46776777 47939116 1162339 gain external link Soueid J, 2016
AutCNV0005142 4 4q13.3 75405778 75521036 115258 loss external link Soueid J, 2016
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
10 46968675 A G PCR or Sanger sequencing Iossifov I, 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
AutLD0000112 10p11.23-q11.23 10 - - 1.89 - Spence, 2006




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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