RGD:150476811 Rat Genome Database

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Variant: RGD:150476811 -  Homo sapiens

RGD ID: 150476811
RS ID: rs72828146
ClinVar ID: CV1279333
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TCF7L2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 114,919,482
GRCh38 10 113,159,723
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001198530.2:c.1147+1654A>G
NM_001146286.2:c.1249+1654A>G
NM_001146285.2:c.1250-197A>G
NM_001198526.2:c.1250-896A>G
More... 		06/14/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TCF7L2
Accession:NM_001146284
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198530
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198529
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198527
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_030756
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198531
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146285
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146283
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001367943
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198526
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001349871
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146274
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198528
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001363501
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001349870
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146286
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198525
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001714042 CLINVAR
dbSNP (RS) rs72828146 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TCF7L2 CLINVAR
OMIM 602228 CLINVAR