| Variant ID | 29197 |
|---|---|
| Entrez Gene ID | 126969 |
| Gene | SLC44A3 (GeneCards) |
| Location | hg19 1:95356667-95356667
hg38 1:94891111-94891111 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | PASM |
| Mutation(HGVS format) | NC_000001.10:g.95356667 C>T (Genome Assembly: GRCh37) |
| Exon or Intron | Intron |
|---|---|
| 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 | 0.2371 |
| CADD Raw score (version 1.3) | -0.238054 (Deleterious) |
| FATHMM raw prediction score | 0.20771 (Tolerated) |
| Deleterious probability by DeFine | 0.5815 (Deleterious) |
| Entrez Gene ID | 126969 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SLC44A3 (GeneCards) |
| Number of variants in SLC44A3 in this database | 2 (view all the variants) |
| Full name | solute carrier family 44 member 3 |
| Band | 1p21.3 |
| Other IDs | Vega: OTTHUMG00000010700 HGNC: HGNC:28689 Ensembl: ENSG00000143036 |
| Other names | CTL3 |
| Summary | None |
| Individual ID | 28503910.74 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28503910 |
| Whose mosaic mutation | Patient |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28503910 |
|---|---|
| Title | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations |
| Journal | Human Mutation |
| Publication date | 2017.05 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 215; |