| Variant ID | 21883 |
|---|---|
| Entrez Gene ID | 51493 |
| Gene | RTCB (GeneCards) |
| Location | hg19 22:32807362-32807362
hg38 22:32411375-32411375 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000022.10:g.32807362 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 | 51304566 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1535 |
| CADD Raw score (version 1.3) | 0.456869 (Deleterious) |
| FATHMM raw prediction score | 0.12751 (Tolerated) |
| Deleterious probability by DeFine | 0.3226 (Neutral) |
| Entrez Gene ID | 51493 (NCBI Gene) |
|---|---|
| Official Gene Symbol | RTCB (GeneCards) |
| Number of variants in RTCB in this database | 4 (view all the variants) |
| Full name | RNA 2',3'-cyclic phosphate and 5'-OH ligase |
| Band | 22q12.3 |
| Other IDs | Vega: OTTHUMG00000030300 OMIM: 613901 HGNC: HGNC:26935 Ensembl: ENSG00000100220 |
| Other names | FAAP, HSPC117, C22orf28, DJ149A16.6 |
| Summary | None |
| Individual ID | 29217584.09 (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; |