| Variant ID | 26924 |
|---|---|
| Entrez Gene ID | 101927575 |
| Gene | LOC101927575 (GeneCards) |
| Location | hg19 9:86717705-86717705
hg38 9:84102790-84102790 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000009.11:g.86717705 A>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 | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0.0011 |
|---|---|
| EIGEN score | -0.4869 |
| CADD Raw score (version 1.3) | -0.490421 (Deleterious) |
| FATHMM raw prediction score | 0.1206 (Tolerated) |
| Deleterious probability by DeFine | 0.3255 (Neutral) |
| Entrez Gene ID | 101927575 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC101927575 (GeneCards) |
| Number of variants in LOC101927575 in this database | 2 (view all the variants) |
| Full name | uncharacterized LOC101927575 |
| Band | 9q21.32 |
| Other IDs | Ensembl: ENSG00000227463 |
| 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 |