| Variant ID | 17752 |
|---|---|
| Entrez Gene ID | 23078 |
| Gene | VWA8 (GeneCards) |
| Location | hg19 13:42152541-42152541
hg38 13:41578405-41578405 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000013.10:g.42152541 C>T (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 | 115169878 |
| MAF in gnomAD genome (version 2.0.1) | 0.00003229 |
|---|---|
| EIGEN score | 0.4405 |
| CADD Raw score (version 1.3) | 1.457884 (Deleterious) |
| FATHMM raw prediction score | 0.1553 (Tolerated) |
| Deleterious probability by DeFine | 0.7448 (Deleterious) |
| Entrez Gene ID | 23078 (NCBI Gene) |
|---|---|
| Official Gene Symbol | VWA8 (GeneCards) |
| Number of variants in VWA8 in this database | 4 (view all the variants) |
| Full name | von Willebrand factor A domain containing 8 |
| Band | 13q14.11 |
| Other IDs | Vega: OTTHUMG00000016799 OMIM: 617509 HGNC: HGNC:29071 Ensembl: ENSG00000102763 |
| Other names | KIAA0564 |
| Summary | None |
| Individual ID | 29217584.15 (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; |