| Variant ID | 26533 |
|---|---|
| Entrez Gene ID | 103724390 |
| Gene | LINC01287 (GeneCards) |
| Location | hg19 7:153412610-153412610
hg38 7:153715525-153715525 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000007.13:g.153412610 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 | 159138663 |
| MAF in gnomAD genome (version 2.0.1) | 0.00006526 |
|---|---|
| EIGEN score | -0.0745 |
| CADD Raw score (version 1.3) | -0.19983 (Deleterious) |
| FATHMM raw prediction score | 0.1088 (Tolerated) |
| Deleterious probability by DeFine | 0.5175 (Deleterious) |
| Entrez Gene ID | 103724390 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01287 (GeneCards) |
| Number of variants in LINC01287 in this database | 3 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1287 |
| Band | 7q36.2 |
| Other IDs | HGNC: HGNC:50351 Ensembl: ENSG00000234722 |
| Other names | TCONS_l2_00027522 |
| 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 |