| Variant ID | 31923 |
|---|---|
| Entrez Gene ID | 170692 |
| Gene | ADAMTS18 (GeneCards) |
| Location | hg19 16:77387705-77387705
hg38 16:77353808-77353808 |
| Disease | Asymptomatic |
| Method | NGS gene panel |
| Mutation(HGVS format) | NC_000016.9:g.77387705 C>T (Genome Assembly: hg19) |
| Exon or Intron | Exon |
|---|---|
| Position in protein | 513 |
| Amino acid changes in protein | Q > Q |
| Position in cDNA | 1539 |
| Changes in cDNA | G > A |
| mRNA accession | NA |
| mRNA length | NA |
| Reference length | 90354753 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| Variant IDs in COSMIC (version 89) | 3512505 |
| Variant occurences in COSMIC | 1(skin) |
| EIGEN score | 1.9269 |
| CADD Raw score (version 1.3) | 0.872331 (Deleterious) |
| FATHMM raw prediction score | 0.97014 (Tolerated) |
| Deleterious probability by DeFine | 0.9667 (Deleterious) |
| Entrez Gene ID | 170692 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ADAMTS18 (GeneCards) |
| Number of variants in ADAMTS18 in this database | 68 (view all the variants) |
| Full name | ADAM metallopeptidase with thrombospondin type 1 motif 18 |
| Band | 16q23.1 |
| Other IDs | Vega: OTTHUMG00000137619 OMIM: 607512 HGNC: HGNC:17110 Ensembl: ENSG00000140873 |
| Other names | KNO2, MMCAT, ADAMTS21 |
| Summary | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may regulate hemostatic balance and function as a tumor suppressor. Mutations in this gene may be associated with microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) and cone-rod dystrophy in human patients. [provided by RefSeq, May 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; |