| Variant ID | 21765 |
|---|---|
| Entrez Gene ID | 118421 |
| Gene | LINC00161 (GeneCards) |
| Location | hg19 21:30191782-30191782
hg38 21:28819460-28819460 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000021.8:g.30191782 C>G (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 | 48129895 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.0502 |
| CADD Raw score (version 1.3) | 0.743269 (Deleterious) |
| FATHMM raw prediction score | 0.13511 (Tolerated) |
| Deleterious probability by DeFine | 0.4384 (Neutral) |
| Entrez Gene ID | 118421 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC00161 (GeneCards) |
| Number of variants in LINC00161 in this database | 6 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 161 |
| Band | 21q21.3 |
| Other IDs | HGNC: HGNC:17138 Ensembl: ENSG00000226935 |
| Other names | C21orf100, Linc-USP16, NCRNA00161 |
| Summary | None |
| Individual ID | 29217584.17 (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; |