RGD:14715572 Rat Genome Database

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Variant: RGD:14715572 -  Homo sapiens

RGD ID: 14715572
RS ID: rs55640037
ClinVar ID: CV660748
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: WFS1  
Reference Nucleotide: -
Variant Nucleotide: AGGGGCATG
Position
Assembly Chr Position
GRCh37 4 6,292,755
GRCh38 4 6,291,028
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145853.1:c.461-169_461-168insAGGGGCATG
NC_000004.11:g.6292755_6292756insAGGGGCATG
NM_006005.3:c.461-169_461-168insAGGGGCATG
NG_011700.1:g.26179_26180insAGGGGCATG
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WFS1
Accession:NM_006005
Location:INTRON

Gene Symbol:WFS1
Accession:NM_001145853
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829433 CLINVAR
dbSNP (RS) rs55640037 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WFS1 CLINVAR
OMIM 606201 CLINVAR