| Variant ID | 28723 |
|---|---|
| Entrez Gene ID | 101929539 |
| Gene | LINC01422 (GeneCards) |
| Location | hg19 22:28073091-28073091
hg38 22:27677094-27677094 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000022.10:g.28073091 C>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 | 51304566 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.5247 |
| CADD Raw score (version 1.3) | 1.04148 (Deleterious) |
| FATHMM raw prediction score | 0.66815 (Tolerated) |
| Deleterious probability by DeFine | 0.4405 (Neutral) |
| Entrez Gene ID | 101929539 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC01422 (GeneCards) |
| Number of variants in LINC01422 in this database | 17 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 1422 |
| Band | 22q12.1 |
| Other IDs | HGNC: HGNC:50728 Ensembl: ENSG00000235271 |
| 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 |