| Variant ID | 26741 |
|---|---|
| Entrez Gene ID | 102724874 |
| Gene | LOC102724874 (GeneCards) |
| Location | hg19 8:78390429-78390429
hg38 8:77478193-77478193 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000008.10:g.78390429 G>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 | 146364022 |
| MAF in gnomAD genome (version 2.0.1) | 0.0002 |
|---|---|
| EIGEN score | 0.0363 |
| CADD Raw score (version 1.3) | 1.096588 (Deleterious) |
| FATHMM raw prediction score | 0.04951 (Tolerated) |
| Deleterious probability by DeFine | 0.4684 (Neutral) |
| Entrez Gene ID | 102724874 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC102724874 (GeneCards) |
| Number of variants in LOC102724874 in this database | 15 (view all the variants) |
| Full name | uncharacterized LOC102724874 |
| Band | 8q21.13 |
| Other IDs | None: |
| 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 |