RGD:11590383 Rat Genome Database

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Variant: RGD:11590383 -  Homo sapiens

RGD ID: 11590383
RS ID: rs754198978
ClinVar ID: CV297292
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGB  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 155,492,426
GRCh38 4 154,571,274
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.*624C>T
LRG_558:g.13295C>T
NG_008833.1:g.13295C>T
NC_000004.12:g.154571274C>T
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_001382762
Location:3UTRS;EXON

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_001382765
Location:3UTRS;EXON

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

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000318458 CLINVAR
dbSNP (RS) rs754198978 CLINVAR
MedGen C2584774 CLINVAR
NCBI Gene FGB CLINVAR
OMIM 134830 CLINVAR
  202400 CLINVAR