| Variant ID | 29187 |
|---|---|
| Entrez Gene ID | 84465 |
| Gene | MEGF11 (GeneCards) |
| Location | hg19 15:66198459-66198459
hg38 15:65906121-65906121 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | PASM |
| Mutation(HGVS format) | NC_000015.9:g.66198459 G>A (Genome Assembly: GRCh37) |
| 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 | 102531392 |
| MAF in gnomAD genome (version 2.0.1) | 0.00006461 |
|---|---|
| SNP ID (dbSNP ID version 137) | rs201758507 |
| EIGEN score | -0.0706 |
| CADD Raw score (version 1.3) | 5.503061 (Deleterious) |
| FATHMM raw prediction score | 0.90994 (Tolerated) |
| SIFT score | 0.062 (Tolerated) |
| LRT score | 0.784 (Tolerated) |
| MutationTaster score | 0.973 (Deleterious) |
| MutatioinAssessor score | 1.61 (Tolerated) |
| PROVEAN score | -1.39 (Tolerated) |
| MetaSVM score | -0.475 (Tolerated) |
| MetaLR score | 0.409 (Tolerated) |
| MCAP score | 0.074 (Deleterious) |
| FitCons score | 0.615 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 3.51 |
| PhyloP score based on multiple alignment of 100 vertebrates | 2.721 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 10.725 |
| Deleterious probability by iFish2 | 0.4317 (Neutral) |
| Deleterious probability by DeFine | 0.8999 (Deleterious) |
| Entrez Gene ID | 84465 (NCBI Gene) |
|---|---|
| Official Gene Symbol | MEGF11 (GeneCards) |
| Number of variants in MEGF11 in this database | 10 (view all the variants) |
| Full name | multiple EGF like domains 11 |
| Band | 15q22.31 |
| Other IDs | Vega: OTTHUMG00000133175 OMIM: 612454 HGNC: HGNC:29635 Ensembl: ENSG00000157890 |
| Other names | None |
| Summary | None |
| Individual ID | 28503910.64 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28503910 |
| Whose mosaic mutation | Patient |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28503910 |
|---|---|
| Title | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations |
| Journal | Human Mutation |
| Publication date | 2017.05 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 215; |