| Variant ID | 8721 |
|---|---|
| Entrez Gene ID | 6940 |
| Gene | ZNF354A (GeneCards) |
| Location | hg19 5:178148649-178148649
hg38 5:178721648-178721648 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000005.9:g.178148649 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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3313 |
| CADD Raw score (version 1.3) | 0.222599 (Deleterious) |
| FATHMM raw prediction score | 0.08336 (Tolerated) |
| Deleterious probability by DeFine | 0.1352 (Neutral) |
| Entrez Gene ID | 6940 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ZNF354A (GeneCards) |
| Number of variants in ZNF354A in this database | 1 (view all the variants) |
| Full name | zinc finger protein 354A |
| Band | 5q35.3 |
| Other IDs | Vega: OTTHUMG00000130895 OMIM: 602444 HGNC: HGNC:11628 Ensembl: ENSG00000169131 |
| Other names | EZNF, HKL1, KID1, KID-1, TCF17, HEL104 |
| Summary | None |
| Individual ID | 29217584.19 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female Patient |
| Phenotype | 3 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| OMIM ID | 216400 |
| Pubmed ID | 29217584 |
|---|---|
| Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Cockayne syndrome Xeroderma Pigmentosum |
| Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |