Annotation Detail
Information
- Associated Genes
- ERBB3
- Associated Variants
-
ERBB3 c.875-147T>G
(
ENST00000683059.1,
ENST00000683164.1,
ENST00000683018.1,
ENST00000267101.8,
ENST00000415288.6 )
ERBB3 c.875-147T>G ( ENST00000267101.8, ENST00000415288.6, ENST00000683018.1, ENST00000683059.1, ENST00000683164.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001982.4(ERBB3):c.875-147T>G AND not provided
- ClinVar Allele ID
- 1240450
- ClinVar RefSeq Alternation Syntax
- NM_001982.4:c.875-147T>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001650211
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs