| Variant ID | 16129 |
|---|---|
| Entrez Gene ID | 4617 |
| Gene | MYF5 (GeneCards) |
| Location | hg19 12:81126379-81126379
hg38 12:80732600-80732600 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000012.11:g.81126379 T>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 | 133851895 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.2243 |
| CADD Raw score (version 1.3) | 0.065731 (Deleterious) |
| FATHMM raw prediction score | 0.26723 (Tolerated) |
| Deleterious probability by DeFine | 0.4748 (Neutral) |
| Entrez Gene ID | 4617 (NCBI Gene) |
|---|---|
| Official Gene Symbol | MYF5 (GeneCards) |
| Number of variants in MYF5 in this database | 2 (view all the variants) |
| Full name | myogenic factor 5 |
| Band | 12q21.31 |
| Other IDs | Vega: OTTHUMG00000170166 OMIM: 159990 HGNC: HGNC:7565 Ensembl: ENSG00000111049 |
| Other names | bHLHc2 |
| Summary | None |
| Individual ID | 29217584.03 (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; |