RGD:12835168 Rat Genome Database

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Variant: RGD:12835168 -  Homo sapiens

RGD ID: 12835168
RS ID: rs782573720
ClinVar ID: CV379356
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF9  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 62,974,230
GRCh38 X 63,754,350
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001369030.1:c.-38A>T
NM_001369034.1:c.-90A>T
NM_001353922.2:c.31-29639A>T
NM_001353923.1:c.48+808A>T
More... 		07/12/2016 5 prime utr variant|intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:ARHGEF9
Accession:NM_001369040
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369045
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001173480
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001353927
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369030
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369033
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369036
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001353924
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369032
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369039
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369037
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369031
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001353926
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_015185
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001353928
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369034
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369042
Location:5UTRS;EXON

Gene Symbol:ARHGEF9
Accession:NM_001369043
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001369041
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001369044
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001330495
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001369038
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001369035
Location:5UTRS;INTRON

Gene Symbol:ARHGEF9
Accession:NM_001353922
Location:INTRON

Gene Symbol:ARHGEF9
Accession:NM_001353921
Location:INTRON

Gene Symbol:ARHGEF9
Accession:NM_001353923
Location:INTRON

Gene Symbol:ARHGEF9
Accession:NM_001173479
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000421222 CLINVAR
dbSNP (RS) rs782573720 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ARHGEF9 CLINVAR
OMIM 300429 CLINVAR