| Variant ID | 27796 |
|---|---|
| Entrez Gene ID | 101928559 |
| Gene | LINC01467 (GeneCards) |
| Location | hg19 14:83371998-83371998
hg38 14:82905654-82905654 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000014.8:g.83371998 C>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 | 107349540 |
| MAF in gnomAD genome (version 2.0.1) | 0.0006 |
|---|---|
| SNP ID (dbSNP ID version 137) | rs112050275 |
| EIGEN score | -0.0148 |
| CADD Raw score (version 1.3) | 0.250535 (Deleterious) |
| FATHMM raw prediction score | 0.18444 (Tolerated) |
| Deleterious probability by DeFine | 0.4606 (Neutral) |
| Entrez Gene ID | 101928559 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01467 (GeneCards) |
| Number of variants in LINC01467 in this database | 27 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1467 |
| Band | 14q31.1 |
| Other IDs | HGNC: HGNC:50911 Ensembl: ENSG00000258977 |
| Other names | None |
| 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 |