| Variant ID | 18573 |
|---|---|
| Entrez Gene ID | 55218 |
| Gene | EXD2 (GeneCards) |
| Location | hg19 14:69659690-69659690
hg38 14:69192973-69192973 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000014.8:g.69659690 G>A (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 | 107349540 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0426 |
| CADD Raw score (version 1.3) | 0.407822 (Deleterious) |
| FATHMM raw prediction score | 0.08901 (Tolerated) |
| Deleterious probability by DeFine | 0.5706 (Deleterious) |
| Entrez Gene ID | 55218 (NCBI Gene) |
|---|---|
| Official Gene Symbol | EXD2 (GeneCards) |
| Number of variants in EXD2 in this database | 4 (view all the variants) |
| Full name | exonuclease 3'-5' domain containing 2 |
| Band | 14q24.1 |
| Other IDs | Vega: OTTHUMG00000154496 OMIM: 616940 HGNC: HGNC:20217 Ensembl: ENSG00000081177 |
| Other names | EXDL2, C14orf114 |
| Summary | None |
| Individual ID | 29217584.15 (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; |