Overview

Variant ID 29547
Entrez Gene ID 374897
Gene SBSN (GeneCards)
Location hg19 19:36018184-36018184
hg38 19:35527282-35527282
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000019.9:g.36018184 G>A (Genome Assembly: hg19)

Other information

Exon or Intron NA
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 59128983

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.6451
CADD Raw score (version 1.3) 10.293431 (Deleterious)
FATHMM raw prediction score 0.95388 (Tolerated)
MutationTaster score 1 (Deleterious)
FitCons score 0.497 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 4.41
PhyloP score based on multiple alignment of 100 vertebrates 2.381
PhastCons score based on multiple alignment of 100 vertebrates 0.842
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 14.453
Deleterious probability by DeFine 0.8733 (Deleterious)
Entrez Gene ID 374897 (NCBI Gene)
Official Gene Symbol SBSN (GeneCards)
Number of variants in SBSN in this database 1 (view all the variants)
Full name suprabasin
Band 19q13.12
Other IDs Vega: OTTHUMG00000048102
OMIM: 609969
HGNC: HGNC:24950
Ensembl: ENSG00000189001
Other names UNQ698
Summary None

Individual #1

Individual ID 28714951.223 (view all the variants in this individual)
Pubmed ID 28714951
Whose mosaic mutation Patient  
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28714951

Pubmed ID 28714951
Title Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
Journal Nat Neurosci
Publication date 2017.07
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 376;