Annotation Detail
Information
- Associated Genes
- EGF
- Associated Variants
-
EGF c.-382A>G
(
ENST00000265171.10,
ENST00000509793.5,
ENST00000652245.1 )
EGF c.-382A>G ( ENST00000265171.10, ENST00000509793.5, ENST00000652245.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001963.6(EGF):c.-382A>G AND not provided
- ClinVar Allele ID
- 227748
- ClinVar RefSeq Alternation Syntax
- NM_001357021.2:c.-382A>G
- ClinVar RefSeq Alternation Syntax
- NM_001178130.3:c.-382A>G
- ClinVar RefSeq Alternation Syntax
- NM_001963.6:c.-382A>G
- ClinVar RefSeq Alternation Syntax
- NM_001178131.3:c.-382A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001723790
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs