| Variant ID | 2623 |
|---|---|
| Entrez Gene ID | 148641 |
| Gene | SLC35F3 (GeneCards) |
| Location | hg19 1:234150144-234150144
hg38 1:234014398-234014398 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000001.10:g.234150144 C>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 | 249250621 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.0069 |
| CADD Raw score (version 1.3) | 0.539132 (Deleterious) |
| FATHMM raw prediction score | 0.18248 (Tolerated) |
| Deleterious probability by DeFine | 0.0853 (Neutral) |
| Entrez Gene ID | 148641 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SLC35F3 (GeneCards) |
| Number of variants in SLC35F3 in this database | 5 (view all the variants) |
| Full name | solute carrier family 35 member F3 |
| Band | 1q42.2 |
| Other IDs | Vega: OTTHUMG00000037929 HGNC: HGNC:23616 Ensembl: ENSG00000183780 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.16 (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; |