Annotation Detail
Information
- Associated Genes
- LZTR1
- Associated Variants
-
LZTR1 p.Arg688Cys (p.R688C)
(
ENST00000646124.2,
ENST00000700578.1 )
LZTR1 p.Arg688Cys (p.R688C) ( ENST00000646124.2, ENST00000700578.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_006767.4(LZTR1):c.2062C>T (p.Arg688Cys) AND not provided
- ClinVar Allele ID
- 106801
- ClinVar RefSeq Alternation Syntax
- NM_006767.4:c.2062C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-10-11
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001055087
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs