Annotation Detail
Information
- Associated Genes
- TXN2
- Associated Variants
-
TXN2 c.387+30A>C
(
ENST00000216185.7,
ENST00000403313.5,
ENST00000416967.1 )
TXN2 c.387+30A>C ( ENST00000216185.7, ENST00000403313.5, ENST00000416967.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_012473.4(TXN2):c.387+30A>C AND not provided
- ClinVar Allele ID
- 1272765
- ClinVar RefSeq Alternation Syntax
- NM_012473.4:c.387+30A>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-05-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001688688
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs