Annotation Detail
Information
- Associated Genes
- TERT
- Associated Variants
-
TERT p.Thr726Met (p.T726M)
(
ENST00000310581.10,
ENST00000334602.10 )
TERT p.Thr726Met (p.T726M) ( ENST00000310581.10, ENST00000334602.10 ) - Associated Disease
- TERT-related disorder
- Source Database
- ClinVar
- Description
- NM_198253.3(TERT):c.2177C>T (p.Thr726Met) AND TERT-related disorder
- ClinVar Allele ID
- 47717
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.2177C>T
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.2177C>T
- ClinVar RefSeq Alternation Syntax
- NR_149162.3:n.2256C>T
- ClinVar RefSeq Alternation Syntax
- NR_149163.3:n.2220C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-03-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004532476
- ClinVar Disease
- TERT-related disorder
- Observed Origin Sample
- germline
Drugs