| Variant ID | 28233 |
|---|---|
| Entrez Gene ID | 729159 |
| Gene | LOC729159 (GeneCards) |
| Location | hg19 16:60663290-60663290
hg38 16:60629386-60629386 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000016.9:g.60663290 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 | 90354753 |
| MAF in gnomAD genome (version 2.0.1) | 0.0015 |
|---|---|
| SNP ID (dbSNP ID version 137) | rs139786183 |
| EIGEN score | -0.5651 |
| CADD Raw score (version 1.3) | -0.213918 (Deleterious) |
| FATHMM raw prediction score | 0.07348 (Tolerated) |
| Deleterious probability by DeFine | 0.1698 (Neutral) |
| Entrez Gene ID | 729159 (NCBI Gene) |
|---|---|
| Official Gene Symbol | LOC729159 (GeneCards) |
| Number of variants in LOC729159 in this database | 8 (view all the variants) |
| Full name | UPF0607 protein ENSP00000381418-like |
| Band | 16q21 |
| Other IDs | Vega: OTTHUMG00000189254 Ensembl: ENSG00000278499 |
| 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 |