| Variant ID | 21983 |
|---|---|
| Entrez Gene ID | 23112 |
| Gene | TNRC6B (GeneCards) |
| Location | hg19 22:40721587-40721587
hg38 22:40325583-40325583 |
| Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000022.10:g.40721587 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) | 0.0000969 |
|---|---|
| EIGEN score | 1.4745 |
| CADD Raw score (version 1.3) | 1.102796 (Deleterious) |
| FATHMM raw prediction score | 0.2268 (Tolerated) |
| Deleterious probability by DeFine | 0.8168 (Deleterious) |
| Entrez Gene ID | 23112 (NCBI Gene) |
|---|---|
| Official Gene Symbol | TNRC6B (GeneCards) |
| Number of variants in TNRC6B in this database | 3 (view all the variants) |
| Full name | trinucleotide repeat containing 6B |
| Band | 22q13.1 |
| Other IDs | Vega: OTTHUMG00000151114 OMIM: 610740 HGNC: HGNC:29190 Ensembl: ENSG00000100354 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.22 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female Patient |
| Phenotype | 3 |
| Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
| OMIM ID | 278700 |
| 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; |