| Variant ID | 2765 |
|---|---|
| Entrez Gene ID | 79573 |
| Gene | TTC13 (GeneCards) |
| Location | hg19 1:231046782-231046782
hg38 1:230911036-230911036 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000001.10:g.231046782 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 | 249250621 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0393 |
| CADD Raw score (version 1.3) | 0.486007 (Deleterious) |
| FATHMM raw prediction score | 0.08632 (Tolerated) |
| Deleterious probability by DeFine | 0.3552 (Neutral) |
| Entrez Gene ID | 79573 (NCBI Gene) |
|---|---|
| Official Gene Symbol | TTC13 (GeneCards) |
| Number of variants in TTC13 in this database | 2 (view all the variants) |
| Full name | tetratricopeptide repeat domain 13 |
| Band | 1q42.2 |
| Other IDs | Vega: OTTHUMG00000037788 HGNC: HGNC:26204 Ensembl: ENSG00000143643 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.21 (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; |