| Variant ID | 8774 |
|---|---|
| Entrez Gene ID | 103724389 |
| Gene | LINC01170 (GeneCards) |
| Location | hg19 5:123473380-123473380
hg38 5:124137687-124137687 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000005.9:g.123473380 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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.0831 |
| CADD Raw score (version 1.3) | 0.091173 (Deleterious) |
| FATHMM raw prediction score | 0.15475 (Tolerated) |
| Deleterious probability by DeFine | 0.6604 (Deleterious) |
| Entrez Gene ID | 103724389 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01170 (GeneCards) |
| Number of variants in LINC01170 in this database | 5 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1170 |
| Band | 5q23.2 |
| Other IDs | HGNC: HGNC:49542 |
| 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; |