RGD:11657938 Rat Genome Database

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Variant: RGD:11657938 -  Homo sapiens

RGD ID: 11657938
RS ID: rs886059144
ClinVar ID: CV297223
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGB  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 155,493,211
GRCh38 4 154,572,059
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Prevalence Trait Synonyms
LRG_558t1:c.*1409C>A
LRG_558:g.14080C>A
NG_008833.1:g.14080C>A
NC_000004.12:g.154572059C>A
More... 		01/12/2018 3 prime utr variant uncertain significance 1-9 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FGB
Accession:NM_001382763
Location:3UTRS;EXON

Gene Symbol:FGB
Accession:NM_001382762
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_001382760
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_001382765
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000345442 CLINVAR
dbSNP (RS) rs886059144 CLINVAR
MedGen C2584774 CLINVAR
NCBI Gene FGB CLINVAR
OMIM 134830 CLINVAR
  202400 CLINVAR