| Variant ID | 21733 |
|---|---|
| Entrez Gene ID | 388815 |
| Gene | MIR99AHG (GeneCards) |
| Location | hg19 21:17778127-17778127
hg38 21:16405807-16405807 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000021.8:g.17778127 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 | 48129895 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.3833 |
| CADD Raw score (version 1.3) | -0.175788 (Deleterious) |
| FATHMM raw prediction score | 0.09962 (Tolerated) |
| Deleterious probability by DeFine | 0.2252 (Neutral) |
| Entrez Gene ID | 388815 (NCBI Gene) |
|---|---|
| Official Gene Symbol | MIR99AHG (GeneCards) |
| Number of variants in MIR99AHG in this database | 14 (view all the variants) |
| Full name | mir-99a-let-7c cluster host gene |
| Band | 21q21.1 |
| Other IDs | OMIM: 615964 HGNC: HGNC:1274 |
| Other names | MONC, C21orf34, C21orf35, LINC00478 |
| Summary | None |
| Individual ID | 29217584.14 (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; |