Annotation Detail
Information
- Associated Genes
- TLR3
- Associated Variants
-
TLR3 p.Phe459= (p.F459=)
(
ENST00000296795.8,
ENST00000504367.1,
ENST00000508051.2,
ENST00000512264.1,
ENST00000698351.1,
ENST00000698354.1 )
TLR3 p.Phe459= (p.F459=) ( ENST00000296795.8, ENST00000504367.1, ENST00000508051.2, ENST00000512264.1, ENST00000698351.1, ENST00000698354.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_003265.3(TLR3):c.1377C>T (p.Phe459=) AND not specified
- ClinVar Allele ID
- 389663
- ClinVar RefSeq Alternation Syntax
- NM_003265.3:c.1377C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000454544
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs