| Variant ID | 23235 |
|---|---|
| Entrez Gene ID | 100129460 |
| Gene | DPY19L1P1 (GeneCards) |
| Location | hg19 7:32661171-32661171
hg38 7:32621559-32621559 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000007.13:g.32661171 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 | 159138663 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0259 |
| CADD Raw score (version 1.3) | 0.591504 (Deleterious) |
| FATHMM raw prediction score | 0.08497 (Tolerated) |
| Deleterious probability by DeFine | 0.337 (Neutral) |
| Entrez Gene ID | 100129460 (NCBI Gene) |
|---|---|
| Official Gene Symbol | DPY19L1P1 (GeneCards) |
| Number of variants in DPY19L1P1 in this database | 2 (view all the variants) |
| Full name | DPY19L1 pseudogene 1 |
| Band | 7p14.3 |
| Other IDs | HGNC: HGNC:22395 |
| Other names | None |
| Summary | None |
| Individual ID | 29217587.01 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 29217587 |
|---|---|
| Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Asymptomatic |
| Number of cases | cases of unknown sex: 3; |