| Variant ID | 18015 |
|---|---|
| Entrez Gene ID | 26153 |
| Gene | KIF26A (GeneCards) |
| Location | hg19 14:104877021-104877021
hg38 14:104410684-104410684 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000014.8:g.104877021 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 | 107349540 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1618 |
| CADD Raw score (version 1.3) | 0.417844 (Deleterious) |
| FATHMM raw prediction score | 0.41269 (Tolerated) |
| Deleterious probability by DeFine | 0.1234 (Neutral) |
| Entrez Gene ID | 26153 (NCBI Gene) |
|---|---|
| Official Gene Symbol | KIF26A (GeneCards) |
| Number of variants in KIF26A in this database | 2 (view all the variants) |
| Full name | kinesin family member 26A |
| Band | 14q32.33 |
| Other IDs | Vega: OTTHUMG00000154986 OMIM: 613231 HGNC: HGNC:20226 Ensembl: ENSG00000066735 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.01 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |