| Variant ID | 29932 |
|---|---|
| Entrez Gene ID | 57573 |
| Gene | ZNF471 (GeneCards) |
| Location | hg19 19:57035824-57035824
hg38 19:56524455-56524455 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | NextSeq500 |
| Mutation(HGVS format) | NC_000019.9:g.57035824 C>A (Genome Assembly: hg19) |
| Exon or Intron | Exon |
|---|---|
| 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 |
|---|---|
| EIGEN score | -1.1368 |
| CADD Raw score (version 1.3) | 0.921456 (Deleterious) |
| FATHMM raw prediction score | 0.14396 (Tolerated) |
| SIFT score | 0.195 (Tolerated) |
| MutationTaster score | 1 (Tolerated) |
| MutatioinAssessor score | 0.975 (Tolerated) |
| PROVEAN score | -0.72 (Tolerated) |
| MetaSVM score | -0.929 (Tolerated) |
| MetaLR score | 0.009 (Tolerated) |
| MCAP score | 0.001 (Tolerated) |
| FitCons score | 0.554 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | -6.34 |
| PhyloP score based on multiple alignment of 100 vertebrates | -2.473 |
| PhastCons score based on multiple alignment of 100 vertebrates | 0 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 4.957 |
| Deleterious probability by iFish2 | 0.0381 (Neutral) |
| Deleterious probability by DeFine | 0.3878 (Neutral) |
| Entrez Gene ID | 57573 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ZNF471 (GeneCards) |
| Number of variants in ZNF471 in this database | 1 (view all the variants) |
| Full name | zinc finger protein 471 |
| Band | 19q13.43 |
| Other IDs | Vega: OTTHUMG00000181943 HGNC: HGNC:23226 Ensembl: ENSG00000196263 |
| Other names | ERP1, Z1971 |
| Summary | None |
| Individual ID | 28867142.23 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28867142 |
| Whose mosaic mutation | Male Patient |
| Origin of mosaic mutation in patients | de novo |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28867142 |
|---|---|
| Title | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
| Journal | American Journal of Human Genetics |
| Publication date | 2017.08 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 247; |