| Variant ID | 25836 |
|---|---|
| Entrez Gene ID | 101927075 |
| Gene | FGF10-AS1 (GeneCards) |
| Location | hg19 5:44431575-44431575
hg38 5:44431473-44431473 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000005.9:g.44431575 G>T (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 | 180915260 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.041 |
| CADD Raw score (version 1.3) | 0.653599 (Deleterious) |
| FATHMM raw prediction score | 0.14068 (Tolerated) |
| Deleterious probability by DeFine | 0.4798 (Neutral) |
| Entrez Gene ID | 101927075 (NCBI Gene) |
|---|---|
| Official Gene Symbol | FGF10-AS1 (GeneCards) |
| Number of variants in FGF10-AS1 in this database | 6 (view all the variants) |
| Full name | FGF10 antisense RNA 1 |
| Band | 5p12 |
| Other IDs | HGNC: HGNC:49382 Ensembl: ENSG00000248464 |
| Other names | None |
| Summary | None |
| Individual ID | 29217587.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |