Annotation Detail
Information
- Associated Genes
- F11 F11-AS1
- Associated Variants
-
F11 p.Ile618Ser (p.I618S)
(
ENST00000403665.7 )
F11 p.Ile618Ser (p.I618S) ( ENST00000403665.7 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000128.4(F11):c.1853T>G (p.Ile618Ser) AND not provided
- ClinVar Allele ID
- 79081
- ClinVar RefSeq Alternation Syntax
- NR_033900.1:n.905A>C
- ClinVar RefSeq Alternation Syntax
- NM_000128.4:c.1853T>G
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000059022
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs