RGD:150474182 Rat Genome Database

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Variant: RGD:150474182 -  Homo sapiens

RGD ID: 150474182
RS ID: rs111824940
ClinVar ID: CV1234406
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TCF7L2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 114,777,657
GRCh38 10 113,017,898
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363501.2:c.451-22127G>A
NM_001367943.1:c.451-22127G>A
NG_012631.1:g.72649G>A
NC_000010.11:g.113017898G>A
More... 		06/15/2019 intron variant benign none provided

Variant Details
Variant Transcripts
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_001198527
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198526
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198531
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146284
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146283
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198525
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001349870
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146285
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001349871
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198529
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001367943
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_030756
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001146286
Location:INTRON

Gene Symbol:TCF7L2
Accession:NM_001198530
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001651726 CLINVAR
dbSNP (RS) rs111824940 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TCF7L2 CLINVAR
OMIM 602228 CLINVAR