| Variant ID | 25091 |
|---|---|
| Entrez Gene ID | 152110 |
| Gene | NEK10 (GeneCards) |
| Location | hg19 3:27285819-27285819
hg38 3:27244328-27244328 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000003.11:g.27285819 G>T (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 | 198022430 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.0916 |
| CADD Raw score (version 1.3) | 0.142735 (Deleterious) |
| FATHMM raw prediction score | 0.21238 (Tolerated) |
| Deleterious probability by DeFine | 0.2387 (Neutral) |
| Entrez Gene ID | 152110 (NCBI Gene) |
|---|---|
| Official Gene Symbol | NEK10 (GeneCards) |
| Number of variants in NEK10 in this database | 5 (view all the variants) |
| Full name | NIMA related kinase 10 |
| Band | 3p24.1 |
| Other IDs | Vega: OTTHUMG00000130571 HGNC: HGNC:18592 Ensembl: ENSG00000163491 |
| Other names | None |
| Summary | None |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |