| Variant ID | 13695 |
|---|---|
| Entrez Gene ID | 23446 |
| Gene | SLC44A1 (GeneCards) |
| Location | hg19 9:108066332-108066332
hg38 9:105304051-105304051 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000009.11:g.108066332 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 | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1725 |
| CADD Raw score (version 1.3) | 0.110712 (Deleterious) |
| FATHMM raw prediction score | 0.2105 (Tolerated) |
| Deleterious probability by DeFine | 0.4781 (Neutral) |
| Entrez Gene ID | 23446 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SLC44A1 (GeneCards) |
| Number of variants in SLC44A1 in this database | 1 (view all the variants) |
| Full name | solute carrier family 44 member 1 |
| Band | 9q31.1-q31.2 |
| Other IDs | Vega: OTTHUMG00000020421 OMIM: 606105 HGNC: HGNC:18798 Ensembl: ENSG00000070214 |
| Other names | CD92, CTL1, CDW92, CHTL1 |
| 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; |