| Variant ID | 12624 |
|---|---|
| Entrez Gene ID | 90362 |
| Gene | FAM110B (GeneCards) |
| Location | hg19 8:59166112-59166112
hg38 8:58253553-58253553 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000008.10:g.59166112 G>C (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 | -0.4597 |
| CADD Raw score (version 1.3) | -0.47802 (Deleterious) |
| FATHMM raw prediction score | 0.06484 (Tolerated) |
| Deleterious probability by DeFine | 0.2222 (Neutral) |
| Entrez Gene ID | 90362 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAM110B (GeneCards) |
| Number of variants in FAM110B in this database | 2 (view all the variants) |
| Full name | family with sequence similarity 110 member B |
| Band | 8q12.1 |
| Other IDs | Vega: OTTHUMG00000164282 OMIM: 611394 HGNC: HGNC:28587 Ensembl: ENSG00000169122 |
| Other names | C8orf72 |
| Summary | None |
| Individual ID | 29217584.17 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female Patient |
| Phenotype | 3 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| OMIM ID | 216400 |
| 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; |