| Variant ID | 22902 |
|---|---|
| Entrez Gene ID | 57495 |
| Gene | NWD2 (GeneCards) |
| Location | hg19 4:37345176-37345176
hg38 4:37343554-37343554 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000004.11:g.37345176 T>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 | 191154276 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.096 |
| CADD Raw score (version 1.3) | 0.063194 (Deleterious) |
| FATHMM raw prediction score | 0.17693 (Tolerated) |
| Deleterious probability by DeFine | 0.7251 (Deleterious) |
| Entrez Gene ID | 57495 (NCBI Gene) |
|---|---|
| Official Gene Symbol | NWD2 (GeneCards) |
| Number of variants in NWD2 in this database | 8 (view all the variants) |
| Full name | NACHT and WD repeat domain containing 2 |
| Band | 4p14 |
| Other IDs | Vega: OTTHUMG00000157134 HGNC: HGNC:29229 Ensembl: ENSG00000174145 |
| Other names | KIAA1239 |
| Summary | None |
| Individual ID | 29217587.01 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 29217587 |
|---|---|
| Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Asymptomatic |
| Number of cases | cases of unknown sex: 3; |