RGD:15152763 Rat Genome Database

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Variant: RGD:15152763 -  Homo sapiens

RGD ID: 15152763
RS ID: rs1470442398
ClinVar ID: CV744442
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TG  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 133,984,127
GRCh38 8 132,971,882
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003235.5:c.6055+9G>A
NG_015832.1:g.109923G>A
NC_000008.11:g.132971882G>A
NC_000008.10:g.133984127G>A
More... 		12/14/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TG
Accession:XM_017013793
Location:INTRON

Gene Symbol:TG
Accession:XM_017013799
Location:INTRON

Gene Symbol:TG
Accession:XM_047422166
Location:INTRON

Gene Symbol:TG
Accession:XM_005251038
Location:INTRON

Gene Symbol:TG
Accession:XM_005251040
Location:INTRON

Gene Symbol:TG
Accession:XM_017013796
Location:INTRON

Gene Symbol:TG
Accession:XM_017013798
Location:INTRON

Gene Symbol:TG
Accession:XM_017013794
Location:INTRON

Gene Symbol:TG
Accession:XM_017013795
Location:INTRON

Gene Symbol:TG
Accession:XM_005251042
Location:INTRON

Gene Symbol:TG
Accession:XM_006716622
Location:INTRON

Gene Symbol:TG
Accession:NM_003235
Location:INTRON

Gene Symbol:TG
Accession:XM_017013800
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000901633 CLINVAR
dbSNP (RS) rs1470442398 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TG CLINVAR
OMIM 188450 CLINVAR