| Variant ID | 19249 |
|---|---|
| Entrez Gene ID | 10363 |
| Gene | HMG20A (GeneCards) |
| Location | hg19 15:77724269-77724269
hg38 15:77431927-77431927 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000015.9:g.77724269 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 | 102531392 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0385 |
| CADD Raw score (version 1.3) | 1.066289 (Deleterious) |
| FATHMM raw prediction score | 0.08067 (Tolerated) |
| Deleterious probability by DeFine | 0.1309 (Neutral) |
| Entrez Gene ID | 10363 (NCBI Gene) |
|---|---|
| Official Gene Symbol | HMG20A (GeneCards) |
| Number of variants in HMG20A in this database | 3 (view all the variants) |
| Full name | high mobility group 20A |
| Band | 15q24.3 |
| Other IDs | Vega: OTTHUMG00000143729 OMIM: 605534 HGNC: HGNC:5001 Ensembl: ENSG00000140382 |
| Other names | HMGX1, HMGXB1 |
| 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; |