| Variant ID | 20671 |
|---|---|
| Entrez Gene ID | 64693 |
| Gene | CTAGE1 (GeneCards) |
| Location | hg19 18:20126106-20126106
hg38 18:22546143-22546143 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000018.9:g.20126106 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 | 78077248 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1272 |
| CADD Raw score (version 1.3) | 0.138671 (Deleterious) |
| FATHMM raw prediction score | 0.17659 (Tolerated) |
| Deleterious probability by DeFine | 0.6867 (Deleterious) |
| Entrez Gene ID | 64693 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CTAGE1 (GeneCards) |
| Number of variants in CTAGE1 in this database | 5 (view all the variants) |
| Full name | cutaneous T cell lymphoma-associated antigen 1 |
| Band | 18q11.2 |
| Other IDs | Vega: OTTHUMG00000165867 OMIM: 608856 HGNC: HGNC:24346 Ensembl: ENSG00000212710 |
| Other names | CTAGE, CT21.1, CT21.2, CTAGE-1, CTAGE-2 |
| Summary | None |
| Individual ID | 29217584.16 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female 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; |