| Variant ID | 23375 |
|---|---|
| Entrez Gene ID | 100616530 |
| Gene | C8orf37-AS1 (GeneCards) |
| Location | hg19 8:96453833-96453833
hg38 8:95441605-95441605 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000008.10:g.96453833 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 | 146364022 |
| MAF in gnomAD genome (version 2.0.1) | 0.00003229 |
|---|---|
| EIGEN score | -0.2802 |
| CADD Raw score (version 1.3) | -0.013931 (Deleterious) |
| FATHMM raw prediction score | 0.10173 (Tolerated) |
| Deleterious probability by DeFine | 0.675 (Deleterious) |
| Entrez Gene ID | 100616530 (NCBI Gene) |
|---|---|
| Official Gene Symbol | C8orf37-AS1 (GeneCards) |
| Number of variants in C8orf37-AS1 in this database | 10 (view all the variants) |
| Full name | C8orf37 antisense RNA 1 |
| Band | 8q22.1 |
| Other IDs | HGNC: HGNC:50444 Ensembl: ENSG00000253773 |
| 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; |