Annotation Detail
Information
- Associated Genes
- TLR7
- Associated Variants
-
TLR7 p.Gln11Leu (p.Q11L)
(
ENST00000380659.4 )
TLR7 p.Gln11Leu (p.Q11L) ( ENST00000380659.4 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_016562.4(TLR7):c.32A>T (p.Gln11Leu) AND not specified
- ClinVar Allele ID
- 2071832
- ClinVar RefSeq Alternation Syntax
- NM_016562.4:c.32A>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003491156
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs