RGD:150460064 Rat Genome Database

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Variant: RGD:150460064 -  Homo sapiens

RGD ID: 150460064
RS ID: rs113301975
ClinVar ID: CV1231277
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGDIA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 79,827,163
GRCh38 17 81,869,287
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001185077.3:c.351+43G>A
NM_001185078.3:c.351+43G>A
NM_001301240.2:c.351+43G>A
NM_001301241.2:c.351+43G>A
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARHGDIA
Accession:NM_004309
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301242
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301243
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001185077
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301240
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001301241
Location:INTRON

Gene Symbol:ARHGDIA
Accession:NM_001185078
Location:INTRON

Gene Symbol:ARHGDIA
Accession:XM_011523574
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001640841 CLINVAR
dbSNP (RS) rs113301975 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARHGDIA CLINVAR
OMIM 601925 CLINVAR