| Variant ID | 26532 |
|---|---|
| Entrez Gene ID | 79970 |
| Gene | ZNF767P (GeneCards) |
| Location | hg19 7:149283609-149283609
hg38 7:149586518-149586518 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000007.13:g.149283609 G>C (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 | 159138663 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3756 |
| CADD Raw score (version 1.3) | -0.457125 (Deleterious) |
| FATHMM raw prediction score | 0.06625 (Tolerated) |
| Deleterious probability by DeFine | 0.0724 (Neutral) |
| Entrez Gene ID | 79970 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ZNF767P (GeneCards) |
| Number of variants in ZNF767P in this database | 4 (view all the variants) |
| Full name | zinc finger family member 767, pseudogene |
| Band | 7q36.1 |
| Other IDs | HGNC: HGNC:21884 Ensembl: ENSG00000133624 |
| Other names | ZNF767 |
| 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 |