| Variant ID | 13719 |
|---|---|
| Entrez Gene ID | 54875 |
| Gene | CNTLN (GeneCards) |
| Location | hg19 9:17328555-17328555
hg38 9:17328557-17328557 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000009.11:g.17328555 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 | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.026 |
| CADD Raw score (version 1.3) | 0.199981 (Deleterious) |
| FATHMM raw prediction score | 0.11915 (Tolerated) |
| Deleterious probability by DeFine | 0.4007 (Neutral) |
| Entrez Gene ID | 54875 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CNTLN (GeneCards) |
| Number of variants in CNTLN in this database | 7 (view all the variants) |
| Full name | centlein |
| Band | 9p22.2 |
| Other IDs | Vega: OTTHUMG00000019599 OMIM: 611870 HGNC: HGNC:23432 Ensembl: ENSG00000044459 |
| Other names | C9orf39, C9orf101, bA340N12.1 |
| 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; |