RGD:15098841 Rat Genome Database

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Variant: RGD:15098841 -  Homo sapiens

RGD ID: 15098841
RS ID: rs140703855
ClinVar ID: CV777251
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GOLGA4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 37,379,234
GRCh38 3 37,337,743
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.12:g.37337743C>T
NC_000003.11:g.37379234C>T
NM_001172713.1:c.6441+9C>T
NM_002078.5:c.6396+9C>T
More... 		05/13/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GOLGA4
Accession:NM_001172713
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265070
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265074
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_017006188
Location:INTRON

Gene Symbol:GOLGA4
Accession:NM_001410721
Location:INTRON

Gene Symbol:GOLGA4
Accession:NM_002078
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265071
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_017006184
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447981
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447986
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265072
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265073
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_006713110
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265075
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_011533598
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_024453457
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447980
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447985
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_017006187
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447984
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_005265069
Location:INTRON

Gene Symbol:GOLGA4
Accession:XM_047447983
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000958650 CLINVAR
dbSNP (RS) rs140703855 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GOLGA4 CLINVAR
OMIM 602509 CLINVAR