RGD:15196368 Rat Genome Database

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Variant: RGD:15196368 -  Homo sapiens

RGD ID: 15196368
RS ID: rs116328109
ClinVar ID: CV777478
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127399792  TACC3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 1,732,604
GRCh38 4 1,730,877
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006342.3:c.1386-10G>C
NG_064424.1:g.14388G>C
NC_000004.12:g.1730877G>C
NC_000004.11:g.1732604G>C
More... 		06/05/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TACC3
Accession:XM_017007653
Location:INTRON

Gene Symbol:TACC3
Accession:XM_011513386
Location:INTRON

Gene Symbol:TACC3
Accession:XM_005247930
Location:INTRON

Gene Symbol:TACC3
Accession:XM_047449523
Location:INTRON

Gene Symbol:TACC3
Accession:NM_006342
Location:INTRON

Gene Symbol:TACC3
Accession:NM_001410699
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:TACC3
Accession:XM_005247929
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000956173 CLINVAR
dbSNP (RS) rs116328109 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TACC3 CLINVAR
OMIM 605303 CLINVAR