Annotation Detail
Information
- Associated Genes
- FLT3
- Associated Variants
-
FLT3 p.Thr227Met (p.T227M)
(
ENST00000241453.12 )
FLT3 p.Thr227Met (p.T227M) ( ENST00000241453.12 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004119.3(FLT3):c.680C>T (p.Thr227Met) AND not provided
- ClinVar Allele ID
- 138186
- ClinVar RefSeq Alternation Syntax
- NR_130706.2:n.746C>T
- ClinVar RefSeq Alternation Syntax
- NM_004119.3:c.680C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001657761
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs