Annotation Detail
Information
- Associated Genes
- TERT
- Associated Variants
-
TERT p.Val867Met (p.V867M)
(
ENST00000310581.10,
ENST00000334602.10 )
TERT p.Val791Ile (p.V791I) ( ENST00000310581.10, ENST00000334602.10 )
TERT p.Val867Met (p.V867M) ( ENST00000310581.10, ENST00000334602.10 )
TERT p.Val791Ile (p.V791I) ( ENST00000310581.10, ENST00000334602.10 ) - Associated Disease
- Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1
- Source Database
- ClinVar
- Description
- NM_198253.2(TERT):c.[2371G>A;2599G>A] AND Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1
- ClinVar Allele ID
- 45604
- ClinVar Allele ID
- 45603
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.2599G>A
- ClinVar RefSeq Alternation Syntax
- NR_149162.3:n.2496G>A
- ClinVar RefSeq Alternation Syntax
- NM_001193376.3:c.2371G>A
- ClinVar RefSeq Alternation Syntax
- NR_149163.3:n.2460G>A
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.2599G>A
- ClinVar RefSeq Alternation Syntax
- NM_198253.3:c.2371G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2011-03-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000030627
- ClinVar Disease
- Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1
- Observed Origin Sample
- germline
- Pubmed
- 21483807
Drugs