| Variant ID | 15049 |
|---|---|
| Entrez Gene ID | 1662 |
| Gene | DDX10 (GeneCards) |
| Location | hg19 11:109030855-109030855
hg38 11:109160128-109160128 |
| Disease | Asymptomatic |
| Method | HiSeq 2000 |
| Mutation(HGVS format) | NC_000011.9:g.109030855 C>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 | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1497 |
| CADD Raw score (version 1.3) | 0.796532 (Deleterious) |
| FATHMM raw prediction score | 0.26062 (Tolerated) |
| Deleterious probability by DeFine | 0.0878 (Neutral) |
| Entrez Gene ID | 1662 (NCBI Gene) |
|---|---|
| Official Gene Symbol | DDX10 (GeneCards) |
| Number of variants in DDX10 in this database | 6 (view all the variants) |
| Full name | DEAD-box helicase 10 |
| Band | 11q22.3 |
| Other IDs | Vega: OTTHUMG00000166540 OMIM: 601235 HGNC: HGNC:2735 Ensembl: ENSG00000178105 |
| Other names | Dbp4, HRH-J8 |
| Summary | DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, and it may be involved in ribosome assembly. Fusion of this gene and the nucleoporin gene, NUP98, by inversion 11 (p15q22) chromosome translocation is found in the patients with de novo or therapy-related myeloid malignancies. [provided by RefSeq, Jul 2008] |
| Individual ID | 29217584.04 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |