| Variant ID | 18177 |
|---|---|
| Entrez Gene ID | 57161 |
| Gene | PELI2 (GeneCards) |
| Location | hg19 14:56974923-56974923
hg38 14:56508205-56508205 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000014.8:g.56974923 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 | 107349540 |
| MAF in gnomAD genome (version 2.0.1) | 0.00009692 |
|---|---|
| EIGEN score | -0.03 |
| CADD Raw score (version 1.3) | 0.735476 (Deleterious) |
| FATHMM raw prediction score | 0.11431 (Tolerated) |
| Deleterious probability by DeFine | 0.0887 (Neutral) |
| Entrez Gene ID | 57161 (NCBI Gene) |
|---|---|
| Official Gene Symbol | PELI2 (GeneCards) |
| Number of variants in PELI2 in this database | 6 (view all the variants) |
| Full name | pellino E3 ubiquitin protein ligase family member 2 |
| Band | 14q22.3 |
| Other IDs | Vega: OTTHUMG00000152336 OMIM: 614798 HGNC: HGNC:8828 Ensembl: ENSG00000139946 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.08 (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; |