| Variant ID | 29649 |
|---|---|
| Entrez Gene ID | 57084 |
| Gene | SLC17A6 (GeneCards) |
| Location | hg19 11:22360097-22360097
hg38 11:22338551-22338551 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000011.9:g.22360097 A>G (Genome Assembly: hg19) |
| 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 | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 1.5857 |
| CADD Raw score (version 1.3) | -0.325847 (Deleterious) |
| FATHMM raw prediction score | 0.95139 (Tolerated) |
| Deleterious probability by DeFine | 0.9158 (Deleterious) |
| Entrez Gene ID | 57084 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SLC17A6 (GeneCards) |
| Number of variants in SLC17A6 in this database | 3 (view all the variants) |
| Full name | solute carrier family 17 member 6 |
| Band | 11p14.3 |
| Other IDs | Vega: OTTHUMG00000166063 OMIM: 607563 HGNC: HGNC:16703 Ensembl: ENSG00000091664 |
| Other names | DNPI, VGLUT2 |
| Summary | None |
| Individual ID | 28714951.325 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28714951 |
| Whose mosaic mutation | Patient |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28714951 |
|---|---|
| Title | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder |
| Journal | Nat Neurosci |
| Publication date | 2017.07 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 376; |