| Variant ID | 22508 |
|---|---|
| Entrez Gene ID | 148641 |
| Gene | SLC35F3 (GeneCards) |
| Location | hg19 1:234049007-234049007
hg38 1:233913261-233913261 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000001.10:g.234049007 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 | 249250621 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0059 |
| CADD Raw score (version 1.3) | -0.095326 (Deleterious) |
| FATHMM raw prediction score | 0.16831 (Tolerated) |
| Deleterious probability by DeFine | 0.6455 (Deleterious) |
| 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 | 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; |