| Variant ID | 24868 |
|---|---|
| Entrez Gene ID | 100506474 |
| Gene | LOC100506474 (GeneCards) |
| Location | hg19 2:13910580-13910580
hg38 2:13770455-13770455 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000002.11:g.13910580 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 | 243199373 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.5625 |
| CADD Raw score (version 1.3) | -0.530895 (Deleterious) |
| FATHMM raw prediction score | 0.03928 (Tolerated) |
| Deleterious probability by DeFine | 0.2331 (Neutral) |
| Entrez Gene ID | 100506474 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC100506474 (GeneCards) |
| Number of variants in LOC100506474 in this database | 9 (view all the variants) |
| Full name | uncharacterized LOC100506474 |
| Band | 2p24.3 |
| Other IDs | Ensembl: ENSG00000225649 |
| Other names | None |
| 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 |