RGD:150480668 Rat Genome Database

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Variant: RGD:150480668 -  Homo sapiens

RGD ID: 150480668
RS ID: rs5754
ClinVar ID: CV1208062
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBXA2R  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 3,595,411
GRCh38 19 3,595,413
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001060.6:c.*275A>G
NM_201636.3:c.983+324A>G
LRG_578:g.16421A>G
NG_031943.1:g.14843T>C
More... 		07/10/2018 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TBXA2R
Accession:NM_001060
Location:3UTRS;EXON

Gene Symbol:TBXA2R
Accession:XM_011528214
Location:3UTRS;EXON

Gene Symbol:TBXA2R
Accession:NM_201636
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001590339 CLINVAR
dbSNP (RS) rs5754 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TBXA2R CLINVAR
OMIM 188070 CLINVAR