| Variant ID | 13692 |
|---|---|
| Entrez Gene ID | 203238 |
| Gene | CCDC171 (GeneCards) |
| Location | hg19 9:15586538-15586538
hg38 9:15586540-15586540 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000009.11:g.15586538 A>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 | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.3476 |
| CADD Raw score (version 1.3) | 1.136268 (Deleterious) |
| FATHMM raw prediction score | 0.89211 (Tolerated) |
| Deleterious probability by DeFine | 0.2152 (Neutral) |
| Entrez Gene ID | 203238 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CCDC171 (GeneCards) |
| Number of variants in CCDC171 in this database | 13 (view all the variants) |
| Full name | coiled-coil domain containing 171 |
| Band | 9p22.3 |
| Other IDs | Vega: OTTHUMG00000019584 HGNC: HGNC:29828 Ensembl: ENSG00000164989 |
| Other names | C9orf93, bA536D16.1, bA778P13.1 |
| Summary | None |
| Individual ID | 29217584.19 (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; |