Annotation Detail
Information
- Associated Genes
- GLB1
- Associated Variants
-
GLB1 p.Leu436Phe (p.L436F)
(
ENST00000307363.10,
ENST00000307377.12,
ENST00000399402.7 )
GLB1 p.Leu436Phe (p.L436F) ( ENST00000307363.10, ENST00000307377.12, ENST00000399402.7 ) - Associated Disease
- GLB1-related disorder
- Source Database
- ClinVar
- Description
- NM_000404.4(GLB1):c.1306C>T (p.Leu436Phe) AND GLB1-related disorder
- ClinVar Allele ID
- 98802
- ClinVar RefSeq Alternation Syntax
- NM_001135602.3:c.913C>T
- ClinVar RefSeq Alternation Syntax
- NM_000404.4:c.1306C>T
- ClinVar RefSeq Alternation Syntax
- NM_001079811.3:c.1216C>T
- ClinVar RefSeq Alternation Syntax
- NM_001317040.2:c.1450C>T
- ClinVar RefSeq Alternation Syntax
- NM_001393580.1:c.1306C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-04-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004542751
- ClinVar Disease
- GLB1-related disorder
- Observed Origin Sample
- germline
Drugs