| Variant ID | 28779 |
|---|---|
| Entrez Gene ID | 101928469 |
| Gene | MIR325HG (GeneCards) |
| Location | hg19 X:76174860-76174860
hg38 X:76954435-76954435 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000023.10:g.76174860 A>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 | 155270560 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| CADD Raw score (version 1.3) | -0.042814 (Deleterious) |
| FATHMM raw prediction score | 0.04351 (Tolerated) |
| Deleterious probability by DeFine | 0.0468 (Neutral) |
| Entrez Gene ID | 101928469 (NCBI Gene) |
|---|---|
| Official Gene Symbol | MIR325HG (GeneCards) |
| Number of variants in MIR325HG in this database | 12 (view all the variants) |
| Full name | MIR325 host gene |
| Band | Xq13.3-q21.1 |
| Other IDs | HGNC: HGNC:50346 Ensembl: ENSG00000280870 |
| Other names | MIR384HG |
| 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 |