Annotation Detail
Information
- Associated Genes
- TERT
- Associated Variants
-
TERT c.2654+269T>C
(
ENST00000310581.10,
ENST00000334602.10 )
TERT c.2654+269T>C ( ENST00000310581.10, ENST00000334602.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_198253.3(TERT):c.2654+269T>C AND not provided
- ClinVar Allele ID
- 520672
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.2654+269T>C
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.2654+269T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-09-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001613425
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs