Annotation Detail
Information
- Associated Genes
- RAG2
- Associated Variants
-
RAG2 p.Gly35Ala (p.G35A)
(
ENST00000532616.2,
ENST00000529083.2,
ENST00000311485.8,
ENST00000527033.6 )
RAG2 p.Gly35Ala (p.G35A) ( ENST00000311485.8, ENST00000527033.6, ENST00000529083.2, ENST00000532616.2 ) - Associated Disease
- Combined immunodeficiency with skin granulomas severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive
- Source Database
- ClinVar
- Description
- NM_000536.4(RAG2):c.104G>C (p.Gly35Ala) AND multiple conditions
- ClinVar Allele ID
- 45377
- ClinVar RefSeq Alternation Syntax
- NM_000536.4:c.104G>C
- ClinVar RefSeq Alternation Syntax
- NM_001243786.2:c.104G>C
- ClinVar RefSeq Alternation Syntax
- NM_001243785.2:c.104G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000819784
- ClinVar Disease
- Combined immunodeficiency with skin granulomas
- ClinVar Disease
- Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- Observed Origin Sample
- germline
Drugs