Annotation Detail
Information
- Associated Genes
- TERT
- Associated Variants
-
TERT c.1951-205G>A
(
ENST00000310581.10,
ENST00000334602.10 )
TERT c.1951-205G>A ( ENST00000310581.10, ENST00000334602.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_198253.3(TERT):c.1951-205G>A AND not provided
- ClinVar Allele ID
- 227598
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.1951-205G>A
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.1951-205G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-10-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001668373
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs