| Variant ID | 11407 |
|---|---|
| Entrez Gene ID | 84792 |
| Gene | FAM220A (GeneCards) |
| Location | hg19 7:6391252-6391252
hg38 7:6351621-6351621 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000007.13:g.6391252 T>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 | 159138663 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.133 |
| CADD Raw score (version 1.3) | 0.079396 (Deleterious) |
| FATHMM raw prediction score | 0.10077 (Tolerated) |
| Deleterious probability by DeFine | 0.2459 (Neutral) |
| Entrez Gene ID | 84792 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FAM220A (GeneCards) |
| Number of variants in FAM220A in this database | 1 (view all the variants) |
| Full name | family with sequence similarity 220 member A |
| Band | 7p22.1 |
| Other IDs | Vega: OTTHUMG00000122091 OMIM: 616628 HGNC: HGNC:22422 Ensembl: ENSG00000178397 |
| Other names | SIPAR, ACPIN1, C7orf70 |
| Summary | None |
| Individual ID | 29217584.19 (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; |