Annotation Detail
Information
- Associated Genes
- F11
- Associated Variants
-
F11 p.Tyr151Cys (p.Y151C)
(
ENST00000403665.7,
ENST00000492972.6 )
F11 p.Tyr151Cys (p.Y151C) ( ENST00000403665.7, ENST00000492972.6 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000128.4(F11):c.452A>G (p.Tyr151Cys) AND not specified
- ClinVar Allele ID
- 79085
- ClinVar RefSeq Alternation Syntax
- NM_000128.4:c.452A>G
- ClinVar RefSeq Alternation Syntax
- NM_001354804.2:c.452A>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-07-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003323384
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs