| Variant ID | 7242 |
|---|---|
| Entrez Gene ID | 166863 |
| Gene | RBM46 (GeneCards) |
| Location | hg19 4:155783227-155783227
hg38 4:154862075-154862075 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000004.11:g.155783227 A>T (Genome Assembly: GRCh37) |
| 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 | -0.3358 |
| CADD Raw score (version 1.3) | -0.426769 (Deleterious) |
| FATHMM raw prediction score | 0.08346 (Tolerated) |
| Deleterious probability by DeFine | 0.0355 (Neutral) |
| Entrez Gene ID | 166863 (NCBI Gene) |
|---|---|
| Official Gene Symbol | RBM46 (GeneCards) |
| Number of variants in RBM46 in this database | 7 (view all the variants) |
| Full name | RNA binding motif protein 46 |
| Band | 4q32.1 |
| Other IDs | Vega: OTTHUMG00000161543 HGNC: HGNC:28401 Ensembl: ENSG00000151962 |
| Other names | CT68 |
| Summary | None |
| Individual ID | 29217584.20 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Male Patient |
| Phenotype | 3 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| OMIM ID | 216400 |
| Pubmed ID | 29217584 |
|---|---|
| Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Cockayne syndrome Xeroderma Pigmentosum |
| Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |