| Variant ID | 25865 |
|---|---|
| Entrez Gene ID | 340107 |
| Gene | LOC340107 (GeneCards) |
| Location | hg19 5:25655759-25655759
hg38 5:25655650-25655650 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000005.9:g.25655759 G>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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0.0016 |
|---|---|
| SNP ID (dbSNP ID version 137) | rs138246657 |
| EIGEN score | -0.4059 |
| CADD Raw score (version 1.3) | -0.358304 (Deleterious) |
| FATHMM raw prediction score | 0.05627 (Tolerated) |
| Deleterious probability by DeFine | 0.1388 (Neutral) |
| Entrez Gene ID | 340107 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC340107 (GeneCards) |
| Number of variants in LINC02239 in this database | 35 (view all the variants) |
| Full name | long intergenic non-protein coding RNA 2239 |
| Band | 5p14.1 |
| Other IDs | HGNC: HGNC:27969 Ensembl: ENSG00000248908 |
| 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 |