Annotation Detail
Information
- Associated Genes
- NOTCH1
- Associated Variants
-
NOTCH1 c.*126G>A
(
ENST00000651671.1,
ENST00000680133.1,
ENST00000680218.1,
ENST00000680668.1,
ENST00000680778.1 )
NOTCH1 c.*126G>A ( ENST00000651671.1, ENST00000680133.1, ENST00000680218.1, ENST00000680668.1, ENST00000680778.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_017617.5(NOTCH1):c.*126G>A AND not provided
- ClinVar Allele ID
- 1247633
- ClinVar RefSeq Alternation Syntax
- NM_017617.5:c.*126G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001673459
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs