RGD:152034486 Rat Genome Database

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Variant: RGD:152034486 -  Homo sapiens

RGD ID: 152034486
RS ID: rs112190652
ClinVar ID: CV1610603
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGDIA  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 79,827,128
GRCh38 17 81,869,252
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301240.2:c.352-16G>A
NM_004309.6:c.352-16G>A
NM_001301243.2:c.487-16G>A
NG_034210.1:g.7155G>A
More...
11/23/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARHGDIA
Accession:NM_001185077
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001185078
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_004309
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301242
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301240
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301243
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301241
Location:INTRON

Gene Symbol:ARHGDIA
Accession:XM_011523574
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NR_125441
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002125105 CLINVAR
dbSNP (RS) rs112190652 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARHGDIA CLINVAR
OMIM 601925 CLINVAR