| Variant ID | 2950 |
|---|---|
| Entrez Gene ID | 55022 |
| Gene | PID1 (GeneCards) |
| Location | hg19 2:229913650-229913650
hg38 2:229048934-229048934 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000002.11:g.229913650 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 | 243199373 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.3628 |
| CADD Raw score (version 1.3) | 0.882942 (Deleterious) |
| FATHMM raw prediction score | 0.19644 (Tolerated) |
| Deleterious probability by DeFine | 0.4866 (Neutral) |
| Entrez Gene ID | 55022 (NCBI Gene) |
|---|---|
| Official Gene Symbol | PID1 (GeneCards) |
| Number of variants in PID1 in this database | 8 (view all the variants) |
| Full name | phosphotyrosine interaction domain containing 1 |
| Band | 2q36.3 |
| Other IDs | Vega: OTTHUMG00000133191 OMIM: 612930 HGNC: HGNC:26084 Ensembl: ENSG00000153823 |
| Other names | PCLI1, NYGGF4, P-CLI1, HMFN2073 |
| Summary | None |
| Individual ID | 29217584.03 (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; |