| Variant ID | 31825 |
|---|---|
| Entrez Gene ID | 4851 |
| Gene | NOTCH1 (GeneCards) |
| Location | hg19 9:139399985-139399986
hg38 9:136505533-136505534 |
| Disease | Asymptomatic |
| Method | NGS gene panel |
| Mutation(HGVS format) | NC_000009.11:g.139399985 GG>AA (Genome Assembly: hg19) |
| Exon or Intron | Exon |
|---|---|
| Position in protein | 1455 |
| Amino acid changes in protein | Q > * |
| Position in cDNA | 4362 |
| Changes in cDNA | C > T |
| mRNA accession | NA |
| mRNA length | NA |
| Reference length | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| Deleterious probability by DeFine | 0.8884 (Deleterious) |
| Entrez Gene ID | 4851 (NCBI Gene) |
|---|---|
| Official Gene Symbol | NOTCH1 (GeneCards) |
| Number of variants in NOTCH1 in this database | 456 (view all the variants) |
| Full name | notch 1 |
| Band | 9q34.3 |
| Other IDs | Vega: OTTHUMG00000020935 OMIM: 190198 HGNC: HGNC:7881 Ensembl: ENSG00000148400 |
| Other names | hN1, AOS5, TAN1, AOVD1 |
| Summary | This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016] |
| Individual ID | 25999502.02 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 25999502 |
| Whose mosaic mutation | Normal |
| Origin of mosaic mutation in patients | de novo |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 25999502 |
|---|---|
| Title | High burden and pervasive positive selection of somatic mutations in normal human skin |
| Journal | Science |
| Publication date | 2015.05 |
| Disease | Asymptomatic |
| Number of cases | Male cases: 1; Female cases: 3; |