Overview

Variant ID 29779
Entrez Gene ID 6586
Gene SLIT3 (GeneCards)
Location hg19 5:168678421-168678421
hg38 5:169251417-169251417
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500
Mutation(HGVS format) NC_000005.9:g.168678421 G>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 1.2896
CADD Raw score (version 1.3) 0.488623 (Deleterious)
FATHMM raw prediction score 0.95414 (Tolerated)
Deleterious probability by DeFine 0.8715 (Deleterious)
Entrez Gene ID 6586 (NCBI Gene)
Official Gene Symbol SLIT3 (GeneCards)
Number of variants in SLIT3 in this database 11 (view all the variants)
Full name slit guidance ligand 3
Band 5q34-q35.1
Other IDs Vega: OTTHUMG00000130409
OMIM: 603745
HGNC: HGNC:11087
Ensembl: ENSG00000184347
Other names MEGF5, SLIL2, SLIT1, slit2, Slit-3
Summary The protein encoded by this gene is secreted, likely interacting with roundabout homolog receptors to effect cell migration. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

Individual #1

Individual ID 28867142.36 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Male Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;