| Variant ID | 28423 |
|---|---|
| Entrez Gene ID | 100505817 |
| Gene | LOC100505817 (GeneCards) |
| Location | hg19 18:71288377-71288377
hg38 18:73621142-73621142 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000018.9:g.71288377 A>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 | 78077248 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.353 |
| CADD Raw score (version 1.3) | 0.035654 (Deleterious) |
| FATHMM raw prediction score | 0.0748 (Tolerated) |
| Deleterious probability by DeFine | 0.3604 (Neutral) |
| Entrez Gene ID | 100505817 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC100505817 (GeneCards) |
| Number of variants in LINC02582 in this database | 12 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 2582 |
| Band | 18q22.3 |
| Other IDs | HGNC: HGNC:53792 Ensembl: ENSG00000261780 |
| Other names | None |
| 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 |