Annotation Detail
Information
- Associated Genes
- FASLG
- Associated Variants
-
FASLG c.395-124A>G
(
ENST00000340030.4,
ENST00000367721.3 )
FASLG c.395-124A>G ( ENST00000340030.4, ENST00000367721.3 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000639.3(FASLG):c.395-124A>G AND not provided
- ClinVar Allele ID
- 1265123
- ClinVar RefSeq Alternation Syntax
- NM_000639.3:c.395-124A>G
- ClinVar RefSeq Alternation Syntax
- NM_001302746.2:c.349-124A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001679116
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs