| Variant ID | 28345 |
|---|---|
| Entrez Gene ID | 55628 |
| Gene | ZNF407 (GeneCards) |
| Location | hg19 18:72689040-72689040
hg38 18:74977084-74977084 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000018.9:g.72689040 C>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 | 78077248 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1532 |
| CADD Raw score (version 1.3) | 0.097355 (Deleterious) |
| FATHMM raw prediction score | 0.17995 (Tolerated) |
| Deleterious probability by DeFine | 0.5555 (Deleterious) |
| Entrez Gene ID | 55628 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ZNF407 (GeneCards) |
| Number of variants in ZNF407 in this database | 10 (view all the variants) |
| Full name | zinc finger protein 407 |
| Band | 18q22.3 |
| Other IDs | Vega: OTTHUMG00000179122 OMIM: 615894 HGNC: HGNC:19904 Ensembl: ENSG00000215421 |
| Other names | None |
| Summary | This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |