RGD:15105012 Rat Genome Database

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Variant: RGD:15105012 -  Homo sapiens

RGD ID: 15105012
RS ID: rs115001709
ClinVar ID: CV731315
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF18  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 7,506,655
GRCh38 19 7,441,769
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367823.1:c.1219+4T>C
NM_001367824.1:c.181+4T>C
NM_015318.4:c.181+4T>C
NM_001130955.2:c.493+4T>C
More... 		11/16/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARHGEF18
Accession:NM_015318
Location:INTRON

Gene Symbol:ARHGEF18
Accession:NM_001130955
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_011527839
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_011527841
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_047438526
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_006722706
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_047438527
Location:INTRON

Gene Symbol:ARHGEF18
Accession:NM_001367824
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_011527837
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_011527836
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_047438528
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XM_005272464
Location:INTRON

Gene Symbol:ARHGEF18
Accession:NM_001367823
Location:INTRON

Gene Symbol:ARHGEF18
Accession:XR_007066705
Location:INTRON;NON-CODING

Gene Symbol:ARHGEF18
Accession:XR_007066706
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000892999 CLINVAR
dbSNP (RS) rs115001709 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARHGEF18 CLINVAR
OMIM 616432 CLINVAR