| Variant ID | 25879 |
|---|---|
| Entrez Gene ID | 404663 |
| Gene | LINC01194 (GeneCards) |
| Location | hg19 5:13426967-13426967
hg38 5:13426855-13426855 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000005.9:g.13426967 G>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 | 0.045 |
| CADD Raw score (version 1.3) | 0.121738 (Deleterious) |
| FATHMM raw prediction score | 0.14608 (Tolerated) |
| Deleterious probability by DeFine | 0.3376 (Neutral) |
| Entrez Gene ID | 404663 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01194 (GeneCards) |
| Number of variants in LINC01194 in this database | 18 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1194 |
| Band | 5p15.2 |
| Other IDs | OMIM: 617097 HGNC: HGNC:37171 |
| Other names | TAG, CT49 |
| Summary | None |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |