| Variant ID | 12023 |
|---|---|
| Entrez Gene ID | 51059 |
| Gene | FAM135B (GeneCards) |
| Location | hg19 8:139186944-139186944
hg38 8:138174701-138174701 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000008.10:g.139186944 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 | 146364022 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.1391 |
| CADD Raw score (version 1.3) | 0.213735 (Deleterious) |
| FATHMM raw prediction score | 0.23493 (Tolerated) |
| Deleterious probability by DeFine | 0.5078 (Deleterious) |
| Entrez Gene ID | 51059 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAM135B (GeneCards) |
| Number of variants in FAM135B in this database | 7 (view all the variants) |
| Full name | family with sequence similarity 135 member B |
| Band | 8q24.23 |
| Other IDs | Vega: OTTHUMG00000149864 HGNC: HGNC:28029 Ensembl: ENSG00000147724 |
| Other names | C8ORFK32 |
| 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; |