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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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 ID | 28714951.223 (view all the variants in this individual) |
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Pubmed ID | 28714951 |
Whose mosaic mutation | Patient |
Phenotype | 3 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
OMIM ID | 209850 |
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; |