Annotation Detail
Information
- Associated Genes
- F11
- Associated Variants
-
F11 p.Gln251Ter (p.Q251*)
(
ENST00000403665.7 )
F11 p.Gln251Ter (p.Q251*) ( ENST00000403665.7 ) - Associated Disease
- Hereditary factor XI deficiency disease
- Source Database
- ClinVar
- Description
- NM_000128.4(F11):c.751C>T (p.Gln251Ter) AND Hereditary factor XI deficiency disease
- ClinVar Allele ID
- 186686
- ClinVar RefSeq Alternation Syntax
- NM_000128.4:c.751C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2014-08-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000169287
- ClinVar Disease
- Hereditary factor XI deficiency disease
- Observed Origin Sample
- unknown
Drugs