Annotation Detail
Information
- Associated Genes
- F11
- Associated Variants
-
F11 p.Cys46Phe (p.C46F)
(
ENST00000403665.7,
ENST00000492972.6 )
F11 p.Cys46Phe (p.C46F) ( ENST00000403665.7, ENST00000492972.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000128.4(F11):c.137G>T (p.Cys46Phe) AND not provided
- ClinVar Allele ID
- 79067
- ClinVar RefSeq Alternation Syntax
- NM_000128.4:c.137G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354804.2:c.137G>T
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000059008
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs