Variant ID | 25981 |
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Entrez Gene ID | 171019 |
Gene | ADAMTS19 (GeneCards) |
Location | hg19 5:128952265-128952265
hg38 5:129616572-129616572 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000005.9:g.128952265 C>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 1.5446 |
CADD Raw score (version 1.3) | 2.339656 (Deleterious) |
FATHMM raw prediction score | 0.97672 (Tolerated) |
Deleterious probability by DeFine | 0.8898 (Deleterious) |
Entrez Gene ID | 171019 (NCBI Gene) |
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Official Gene Symbol | ADAMTS19 (GeneCards) |
Number of variants in ADAMTS19 in this database | 6 (view all the variants) |
Full name | ADAM metallopeptidase with thrombospondin type 1 motif 19 |
Band | 5q23.3 |
Other IDs | Vega: OTTHUMG00000128990 OMIM: 607513 HGNC: HGNC:17111 Ensembl: ENSG00000145808 |
Other names | None |
Summary | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family 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 protein encoded by this gene has high sequence similarity to the protein encoded by ADAMTS16, another family member. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |