Annotation Detail
Information
- Associated Genes
- ADAMTS13
- Associated Variants
-
ADAMTS13 p.Pro618Ala (p.P618A)
(
ENST00000355699.7,
ENST00000356589.6,
ENST00000371916.5,
ENST00000371929.7 )
ADAMTS13 p.Pro618Ala (p.P618A) ( ENST00000355699.7, ENST00000356589.6, ENST00000371916.5, ENST00000371929.7 ) - Associated Disease
- Upshaw-Schulman syndrome
- Source Database
- ClinVar
- Description
- NM_139027.6(ADAMTS13):c.1852C>G (p.Pro618Ala) AND Upshaw-Schulman syndrome
- ClinVar Allele ID
- 253385
- ClinVar RefSeq Alternation Syntax
- NM_139027.6:c.1852C>G
- ClinVar RefSeq Alternation Syntax
- NM_139026.6:c.1759C>G
- ClinVar RefSeq Alternation Syntax
- NM_139025.5:c.1852C>G
- ClinVar RefSeq Alternation Syntax
- NR_024514.3:n.1141C>G
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2016-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000345892
- ClinVar Disease
- Upshaw-Schulman syndrome
- Observed Origin Sample
- germline
Drugs