Annotation Detail
Information
- Associated Genes
- GLI3
- Associated Variants
-
GLI3 p.Glu81Lys (p.E81K)
(
ENST00000395925.8,
ENST00000479210.1,
ENST00000642432.1,
ENST00000647255.1,
ENST00000677288.1,
ENST00000677605.1 )
GLI3 p.Glu81Lys (p.E81K) ( ENST00000395925.8, ENST00000479210.1, ENST00000642432.1, ENST00000647255.1, ENST00000677288.1, ENST00000677605.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000168.6(GLI3):c.241G>A (p.Glu81Lys) AND Inborn genetic diseases
- ClinVar Allele ID
- 259864
- ClinVar RefSeq Alternation Syntax
- NM_000168.6:c.241G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-09-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004021025
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs