| Variant ID | 29578 |
|---|---|
| Entrez Gene ID | 55122 |
| Gene | AKIRIN2 (GeneCards) |
| Location | hg19 6:88385638-88385638
hg38 6:87675920-87675920 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000006.11:g.88385638 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 | 171115067 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1306 |
| CADD Raw score (version 1.3) | 2.836563 (Deleterious) |
| FATHMM raw prediction score | 0.98557 (Tolerated) |
| SIFT score | 0.66 (Tolerated) |
| LRT score | 0 (Deleterious) |
| MutationTaster score | 1 (Deleterious) |
| MutatioinAssessor score | 0.895 (Tolerated) |
| PROVEAN score | -1.02 (Tolerated) |
| MetaSVM score | -0.991 (Tolerated) |
| MetaLR score | 0.084 (Tolerated) |
| MCAP score | 0.002 (Tolerated) |
| FitCons score | 0.707 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 5.77 |
| PhyloP score based on multiple alignment of 100 vertebrates | 3.746 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 20.347 |
| Deleterious probability by iFish2 | 0.1779 (Neutral) |
| Deleterious probability by DeFine | 0.9085 (Deleterious) |
| Entrez Gene ID | 55122 (NCBI Gene) |
|---|---|
| Official Gene Symbol | AKIRIN2 (GeneCards) |
| Number of variants in AKIRIN2 in this database | 2 (view all the variants) |
| Full name | akirin 2 |
| Band | 6q15 |
| Other IDs | Vega: OTTHUMG00000015180 OMIM: 615165 HGNC: HGNC:21407 Ensembl: ENSG00000135334 |
| Other names | FBI1, C6orf166, dJ486L4.2 |
| Summary | None |
| Individual ID | 28714951.254 (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; |