Overview

Variant ID 29355
Entrez Gene ID 57448
Gene BIRC6 (GeneCards)
Location hg19 2:32730150-32730150
hg38 2:32505083-32505083
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000002.11:g.32730150 G>C (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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.961
CADD Raw score (version 1.3) 7.477948 (Deleterious)
FATHMM raw prediction score 0.99521 (Tolerated)
SIFT score 0 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.25 (Deleterious)
PROVEAN score -6.33 (Deleterious)
MetaSVM score 0.572 (Deleterious)
MetaLR score 0.759 (Deleterious)
MCAP score 0.246 (Deleterious)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 6.02
PhyloP score based on multiple alignment of 100 vertebrates 10.003
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 20.541
Deleterious probability by iFish2 0.4611 (Neutral)
Deleterious probability by DeFine 0.9587 (Deleterious)
Entrez Gene ID 57448 (NCBI Gene)
Official Gene Symbol BIRC6 (GeneCards)
Number of variants in BIRC6 in this database 5 (view all the variants)
Full name baculoviral IAP repeat containing 6
Band 2p22.3
Other IDs Vega: OTTHUMG00000150528
OMIM: 605638
HGNC: HGNC:13516
Ensembl: ENSG00000115760
Other names BRUCE, APOLLON
Summary This gene encodes a protein with a BIR (baculoviral inhibition of apoptosis protein repeat) domain and a UBCc (ubiquitin-conjugating enzyme E2, catalytic) domain. This protein inhibits apoptosis by facilitating the degradation of apoptotic proteins by ubiquitination. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 28714951.31 (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;