| Variant ID | 29670 |
|---|---|
| Entrez Gene ID | 54439 |
| Gene | RBM27 (GeneCards) |
| Location | hg19 5:145603023-145603023
hg38 5:146223460-146223460 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000005.9:g.145603023 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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.468 |
| CADD Raw score (version 1.3) | 5.023175 (Deleterious) |
| FATHMM raw prediction score | 0.97227 (Tolerated) |
| SIFT score | 0.039 (Deleterious) |
| LRT score | 0 (Deleterious) |
| MutationTaster score | 1 (Deleterious) |
| MutatioinAssessor score | 2.045 (Deleterious) |
| PROVEAN score | -4.27 (Deleterious) |
| MetaSVM score | -0.847 (Tolerated) |
| MetaLR score | 0.132 (Tolerated) |
| MCAP score | 0.017 (Tolerated) |
| FitCons score | 0.732 (Highly Significant p < 0.003 ) |
| Genomic Evolutionary Rate Profiling (GERP) score | 5.83 |
| PhyloP score based on multiple alignment of 100 vertebrates | 5.114 |
| PhastCons score based on multiple alignment of 100 vertebrates | 1 |
| SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 20.113 |
| Deleterious probability by iFish2 | 0.4695 (Deleterious) |
| Deleterious probability by DeFine | 0.9074 (Deleterious) |
| Entrez Gene ID | 54439 (NCBI Gene) |
|---|---|
| Official Gene Symbol | RBM27 (GeneCards) |
| Number of variants in RBM27 in this database | 2 (view all the variants) |
| Full name | RNA binding motif protein 27 |
| Band | 5q32 |
| Other IDs | Vega: OTTHUMG00000188625 HGNC: HGNC:29243 Ensembl: ENSG00000275740 |
| Other names | Psc1, ARRS1, ZC3H18, ZC3H20 |
| Summary | None |
| Individual ID | 28714951.346 (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; |