Annotation Detail

Information
Associated Genes
RAG2
Associated Variants
RAG2 p.Glu437Lys (p.E437K) ( ENST00000311485.8, ENST00000527033.6, ENST00000532616.2, ENST00000529083.2 )
RAG2 p.Glu437Lys (p.E437K) ( ENST00000311485.8, ENST00000527033.6, ENST00000529083.2, ENST00000532616.2 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000536.4(RAG2):c.1309G>A (p.Glu437Lys) AND not provided
ClinVar Allele ID
45379
ClinVar RefSeq Alternation Syntax
NM_000536.4:c.1309G>A
ClinVar RefSeq Alternation Syntax
NM_001243786.2:c.1309G>A
ClinVar RefSeq Alternation Syntax
NM_001243785.2:c.1309G>A
Clinical Significance Description
Likely pathogenic
Clinical Significance Last Update
2015-12-21
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000413563
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs