| Variant ID | 15805 |
|---|---|
| Entrez Gene ID | 100528017 |
| Gene | SAA2-SAA4 (GeneCards) |
| Location | hg19 11:18254742-18254742
hg38 11:18233195-18233195 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000011.9:g.18254742 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 | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3863 |
| CADD Raw score (version 1.3) | -0.114204 (Deleterious) |
| FATHMM raw prediction score | 0.10504 (Tolerated) |
| Deleterious probability by DeFine | 0.248 (Neutral) |
| Entrez Gene ID | 100528017 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SAA2-SAA4 (GeneCards) |
| Number of variants in SAA2-SAA4 in this database | 1 (view all the variants) |
| Full name | SAA2-SAA4 readthrough |
| Band | 11p15.1 |
| Other IDs | Vega: OTTHUMG00000166482 HGNC: HGNC:39550 Ensembl: ENSG00000255071 |
| Other names | None |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring serum amyloid A2 and serum amyloid A4 genes on chromosome 11. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010] |
| Individual ID | 29217584.16 (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; |