| Variant ID | 29523 |
|---|---|
| Entrez Gene ID | 643641 |
| Gene | ZNF862 (GeneCards) |
| Location | hg19 7:149544968-149544968
hg38 7:149847879-149847879 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000007.13:g.149544968 G>A (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 |
|---|---|
| EIGEN score | -1.1967 |
| CADD Raw score (version 1.3) | -0.890917 (Deleterious) |
| FATHMM raw prediction score | 0.01405 (Tolerated) |
| SIFT score | 0.683 (Tolerated) |
| LRT score | 0.124 (Tolerated) |
| MutationTaster score | 1 (Tolerated) |
| MutatioinAssessor score | 0.63 (Tolerated) |
| PROVEAN score | -0.19 (Tolerated) |
| MetaSVM score | -0.926 (Tolerated) |
| MetaLR score | 0.001 (Tolerated) |
| MCAP score | 0.002 (Tolerated) |
| FitCons score | 0.651 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 0.804 |
| PhyloP score based on multiple alignment of 100 vertebrates | 0.475 |
| PhastCons score based on multiple alignment of 100 vertebrates | 0.001 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 5.246 |
| Deleterious probability by iFish2 | 0.0842 (Neutral) |
| Deleterious probability by DeFine | 0.7646 (Deleterious) |
| Entrez Gene ID | 643641 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ZNF862 (GeneCards) |
| Number of variants in ZNF862 in this database | 1 (view all the variants) |
| Full name | zinc finger protein 862 |
| Band | 7q36.1 |
| Other IDs | Vega: OTTHUMG00000158093 HGNC: HGNC:34519 Ensembl: ENSG00000106479 |
| Other names | None |
| Summary | None |
| Individual ID | 28714951.199 (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 |
| 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; |