RGD:11655200 Rat Genome Database

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Variant: RGD:11655200 -  Homo sapiens

RGD ID: 11655200
RS ID: rs886052653
ClinVar ID: CV327425
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF13B  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 16,852,296
GRCh38 17 16,948,982
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_120t1:c.201G>C
LRG_120:g.28107G>C
NG_007281.1:g.28107G>C
NC_000017.11:g.16948982C>G
More... 		06/14/2016 missense variant uncertain significance ANTIBODY DEFICIENCY DUE TO TACI DEFECT; Hypogamma-globulinemia, acquired; HYPOGAMMAGLOBULINEMIA DUE TO TACI DEFICIENCY; Immunoglobulin deficiency, late-onset
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TNFRSF13B
Accession:NM_012452
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000323777 CLINVAR
  RCV002521095 CLINVAR
dbSNP (RS) rs886052653 CLINVAR
MedGen C3150354 CLINVAR
  CN239265 CLINVAR
NCBI Gene TNFRSF13B CLINVAR
OMIM 240500 CLINVAR
  604907 CLINVAR