Variant ID | 29342 |
---|---|
Entrez Gene ID | 563 |
Gene | AZGP1 (GeneCards) |
Location | hg19 7:99573589-99573589
hg38 7:99975966-99975966 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
Method | MiSeq |
Mutation(HGVS format) | NC_000007.13:g.99573589 C>T (Genome Assembly: hg19) |
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 | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
SNP ID (dbSNP ID version 137) | rs76208463 |
Variant IDs in COSMIC (version 89) | 6330014 |
Variant occurences in COSMIC | 1(liver) |
EIGEN score | -0.8335 |
CADD Raw score (version 1.3) | 2.367593 (Deleterious) |
FATHMM raw prediction score | 0.04171 (Tolerated) |
SIFT score | 0.05 (Deleterious) |
MutationTaster score | 1 (Tolerated) |
MutatioinAssessor score | 2.335 (Deleterious) |
PROVEAN score | -0.5 (Tolerated) |
MetaSVM score | -0.933 (Tolerated) |
MetaLR score | 0.003 (Tolerated) |
MCAP score | 0.003 (Tolerated) |
FitCons score | 0.598 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 1.41 |
PhyloP score based on multiple alignment of 100 vertebrates | 0.039 |
PhastCons score based on multiple alignment of 100 vertebrates | 0 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 5.292 |
Deleterious probability by iFish2 | 0.0226 (Neutral) |
Deleterious probability by DeFine | 0.649 (Deleterious) |
Entrez Gene ID | 563 (NCBI Gene) |
---|---|
Official Gene Symbol | AZGP1 (GeneCards) |
Number of variants in AZGP1 in this database | 1 (view all the variants) |
Full name | alpha-2-glycoprotein 1, zinc-binding |
Band | 7q22.1 |
Other IDs | Vega: OTTHUMG00000023066 OMIM: 194460 HGNC: HGNC:910 Ensembl: ENSG00000160862 |
Other names | ZAG, ZA2G |
Summary | None |
Individual ID | 28714951.18 (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; |