| Variant ID | 10155 |
|---|---|
| Entrez Gene ID | 442229 |
| Gene | SLC25A51P1 (GeneCards) |
| Location | hg19 6:67010506-67010506
hg38 6:66300613-66300613 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000006.11:g.67010506 C>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 | -0.3684 |
| CADD Raw score (version 1.3) | -0.038166 (Deleterious) |
| FATHMM raw prediction score | 0.05934 (Tolerated) |
| Deleterious probability by DeFine | 0.0475 (Neutral) |
| Entrez Gene ID | 442229 (NCBI Gene) |
|---|---|
| Official Gene Symbol | SLC25A51P1 (GeneCards) |
| Number of variants in SLC25A51P1 in this database | 38 (view all the variants) |
| Full name | solute carrier family 25 member 51 pseudogene 1 |
| Band | 6q12 |
| Other IDs | HGNC: HGNC:23325 |
| Other names | MCART3P, bA707M13.1 |
| 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; |