| Variant ID | 21904 |
|---|---|
| Entrez Gene ID | 25771 |
| Gene | TBC1D22A (GeneCards) |
| Location | hg19 22:47504585-47504585
hg38 22:47108689-47108689 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000022.10:g.47504585 T>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 | 51304566 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.392 |
| CADD Raw score (version 1.3) | 0.062254 (Deleterious) |
| FATHMM raw prediction score | 0.06305 (Tolerated) |
| Deleterious probability by DeFine | 0.0589 (Neutral) |
| Entrez Gene ID | 25771 (NCBI Gene) |
|---|---|
| Official Gene Symbol | TBC1D22A (GeneCards) |
| Number of variants in TBC1D22A in this database | 10 (view all the variants) |
| Full name | TBC1 domain family member 22A |
| Band | 22q13.31 |
| Other IDs | Vega: OTTHUMG00000150332 OMIM: 616879 HGNC: HGNC:1309 Ensembl: ENSG00000054611 |
| Other names | C22orf4, HSC79E021 |
| Summary | None |
| Individual ID | 29217584.11 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |