RGD:28882129 Rat Genome Database

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Variant: RGD:28882129 -  Homo sapiens

RGD ID: 28882129
RS ID: rs2227425
ClinVar ID: CV890253
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGB  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 155,492,872
GRCh38 4 154,571,720
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001184741.1:c.*1070G>C
NG_008833.1:g.13741G>C
NC_000004.12:g.154571720G>C
NC_000004.11:g.155492872G>C
More... 		11/15/2017 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FGB
Accession:NM_001382760
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382764
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382761
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001184741
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382759
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_005141
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382762
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382765
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382763
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:22273812  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001149841 CLINVAR
dbSNP (RS) rs2227425 CLINVAR
MedGen C2584774 CLINVAR
NCBI Gene FGB CLINVAR
OMIM 134830 CLINVAR
  202400 CLINVAR