RGD:11606785 Rat Genome Database

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Variant: RGD:11606785 -  Homo sapiens

RGD ID: 11606785
ClinVar ID: CV313226
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TJP2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 71,869,923
GRCh38 9 69,255,007
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.69255007A>G
NC_000009.11:g.71869923A>G
NM_004817.4:c.*633A>G
NG_016342.2:g.159101A>G
More... 		06/14/2016 3 prime utr variant likely benign

Variant Details
Variant Transcripts
Gene Symbol:TJP2
Accession:NM_001369872
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001170415
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_011519209
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001369870
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001369871
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_047424094
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_004817
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_047424095
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001369875
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001369874
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_047424090
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001170416
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_011519208
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_047424092
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001170414
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_201629
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_011519206
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_047424091
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:NM_001369873
Location:3UTRS;EXON

Gene Symbol:TJP2
Accession:XM_011519207
Location:3UTRS;EXON

Variant Samples