| Variant ID | 29103 |
|---|---|
| Entrez Gene ID | 100507528 |
| Gene | LINC00613 (GeneCards) |
| Location | hg19 4:138417312-138417312
hg38 4:137496158-137496158 |
| Disease | Asymptomatic |
| Method | Ultra deep amplicon Sequencing |
| Mutation(HGVS format) | NC_000004.11:g.138417312 G>A (Genome Assembly: hg19) |
| Exon or Intron | Intron |
|---|---|
| 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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.6213 |
| CADD Raw score (version 1.3) | -0.683336 (Deleterious) |
| FATHMM raw prediction score | 0.07743 (Tolerated) |
| Deleterious probability by DeFine | 0.4869 (Neutral) |
| Entrez Gene ID | 100507528 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LINC00613 (GeneCards) |
| Number of variants in LINC00613 in this database | 25 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 613 |
| Band | 4q28.3 |
| Other IDs | HGNC: HGNC:44060 Ensembl: ENSG00000248330 |
| Other names | None |
| Summary | None |
| Individual ID | 29283202.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29283202 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 29283202 |
|---|---|
| Title | Identification of somatic mutations in postmortem human brains by whole genome sequencing and their implications for psychiatric disorders. |
| Journal | Psychiatry Clin Neurosci |
| Publication date | 2018.04 |
| Disease | Asymptomatic |
| Population | Caucasian;Japanese |
| Number of cases | cases of unknown sex: 3; |