| Variant ID | 26756 |
|---|---|
| Entrez Gene ID | 103352670 |
| Gene | LINC01419 (GeneCards) |
| Location | hg19 8:85012568-85012568
hg38 8:84100333-84100333 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000008.10:g.85012568 T>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 | 146364022 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.4081 |
| CADD Raw score (version 1.3) | 0.17031 (Deleterious) |
| FATHMM raw prediction score | 0.09103 (Tolerated) |
| Deleterious probability by DeFine | 0.4013 (Neutral) |
| Entrez Gene ID | 103352670 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01419 (GeneCards) |
| Number of variants in LINC01419 in this database | 10 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1419 |
| Band | 8q21.13 |
| Other IDs | HGNC: HGNC:50712 Ensembl: ENSG00000253898 |
| Other names | LVCAT7, TCONS_00014497 |
| 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 |