| Variant ID | 27722 |
|---|---|
| Entrez Gene ID | 646982 |
| Gene | LINC00598 (GeneCards) |
| Location | hg19 13:40996623-40996623
hg38 13:40422486-40422486 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000013.10:g.40996623 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 | 115169878 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1728 |
| CADD Raw score (version 1.3) | 0.01358 (Deleterious) |
| FATHMM raw prediction score | 0.09462 (Tolerated) |
| Deleterious probability by DeFine | 0.5754 (Deleterious) |
| Entrez Gene ID | 646982 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC00598 (GeneCards) |
| Number of variants in LINC00598 in this database | 5 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 598 |
| Band | 13q14.11 |
| Other IDs | HGNC: HGNC:42770 Ensembl: ENSG00000215483 |
| Other names | lncFOXO1 |
| Summary | None |
| Individual ID | 29217587.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |