Annotation Detail
Information
- Associated Genes
- TERT LOC110806263
- Associated Variants
-
TERT c.219+1G>A
(
ENST00000310581.10,
ENST00000334602.10 )
TERT c.219+1G>A ( ENST00000310581.10, ENST00000334602.10 ) - Associated Disease
- Dyskeratosis congenita, autosomal dominant 2 Idiopathic Pulmonary Fibrosis
- Source Database
- ClinVar
- Description
- NM_198253.3(TERT):c.219+1G>A AND multiple conditions
- ClinVar Allele ID
- 27777
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.219+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.219+1G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2021-08-04
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002513017
- ClinVar Disease
- Idiopathic Pulmonary Fibrosis
- ClinVar Disease
- Dyskeratosis congenita, autosomal dominant 2
- Observed Origin Sample
- germline
Drugs