Annotation Detail
Information
- Associated Genes
- NBN
- Associated Variants
-
NBN c.37+1G>A
(
ENST00000265433.8,
ENST00000523444.2,
ENST00000697292.1,
ENST00000697293.1,
ENST00000697298.1,
ENST00000697299.1,
ENST00000697304.1,
ENST00000697307.1,
ENST00000697308.1,
ENST00000697309.1,
ENST00000697310.1 )
NBN c.37+1G>A ( ENST00000265433.8, ENST00000523444.2, ENST00000697292.1, ENST00000697293.1, ENST00000697298.1, ENST00000697299.1, ENST00000697304.1, ENST00000697307.1, ENST00000697308.1, ENST00000697309.1, ENST00000697310.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002485.5(NBN):c.37+1G>A AND not provided
- ClinVar Allele ID
- 182906
- ClinVar RefSeq Alternation Syntax
- NM_001024688.3:c.-260+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_002485.5:c.37+1G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2022-07-20
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000708614
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs