| Variant ID | 29484 |
|---|---|
| Entrez Gene ID | 79725 |
| Gene | THAP9 (GeneCards) |
| Location | hg19 4:83839760-83839760
hg38 4:82918607-82918607 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000004.11:g.83839760 C>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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.4077 |
| CADD Raw score (version 1.3) | 3.256381 (Deleterious) |
| FATHMM raw prediction score | 0.90564 (Tolerated) |
| SIFT score | 0.019 (Deleterious) |
| LRT score | 0.145 (Tolerated) |
| MutationTaster score | 0.999 (Tolerated) |
| MutatioinAssessor score | 1.04 (Tolerated) |
| PROVEAN score | 0.18 (Tolerated) |
| MetaSVM score | -0.341 (Tolerated) |
| MetaLR score | 0.477 (Tolerated) |
| MCAP score | 0.032 (Deleterious) |
| FitCons score | 0.651 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 2.33 |
| PhyloP score based on multiple alignment of 100 vertebrates | 2.184 |
| PhastCons score based on multiple alignment of 100 vertebrates | 0.97 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 8.261 |
| Deleterious probability by iFish2 | 0.2814 (Neutral) |
| Deleterious probability by DeFine | 0.6453 (Deleterious) |
| Entrez Gene ID | 79725 (NCBI Gene) |
|---|---|
| Official Gene Symbol | THAP9 (GeneCards) |
| Number of variants in THAP9 in this database | 3 (view all the variants) |
| Full name | THAP domain containing 9 |
| Band | 4q21.22 |
| Other IDs | Vega: OTTHUMG00000130291 OMIM: 612537 HGNC: HGNC:23192 Ensembl: ENSG00000168152 |
| Other names | hTh9 |
| Summary | None |
| Individual ID | 28714951.160 (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; |