| Variant ID | 9470 |
|---|---|
| Entrez Gene ID | 79632 |
| Gene | FAM184A (GeneCards) |
| Location | hg19 6:119379781-119379781
hg38 6:119058616-119058616 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000006.11:g.119379781 G>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 | 171115067 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.098 |
| CADD Raw score (version 1.3) | 0.976027 (Deleterious) |
| FATHMM raw prediction score | 0.14777 (Tolerated) |
| Deleterious probability by DeFine | 0.2637 (Neutral) |
| Entrez Gene ID | 79632 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAM184A (GeneCards) |
| Number of variants in FAM184A in this database | 4 (view all the variants) |
| Full name | family with sequence similarity 184 member A |
| Band | 6q22.31 |
| Other IDs | Vega: OTTHUMG00000015471 HGNC: HGNC:20991 Ensembl: ENSG00000111879 |
| Other names | C6orf60 |
| Summary | None |
| Individual ID | 29217584.10 (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; |