Annotation Detail
Information
- Associated Genes
- ADAMTS13
- Associated Variants
-
ADAMTS13 p.Ala732Val (p.A732V)
(
ENST00000355699.7,
ENST00000356589.6,
ENST00000371916.5,
ENST00000371929.7 )
ADAMTS13 p.Ala732Val (p.A732V) ( ENST00000355699.7, ENST00000356589.6, ENST00000371916.5, ENST00000371929.7 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_139027.6(ADAMTS13):c.2195C>T (p.Ala732Val) AND not specified
- ClinVar Allele ID
- 229677
- ClinVar RefSeq Alternation Syntax
- NM_139025.5:c.2195C>T
- ClinVar RefSeq Alternation Syntax
- NM_139027.6:c.2195C>T
- ClinVar RefSeq Alternation Syntax
- NM_139026.6:c.2102C>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2023-08-15
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000220213
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs