RGD:8651978 Rat Genome Database

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Variant: RGD:8651978 -  Homo sapiens

RGD ID: 8651978
ClinVar ID: CV128553
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP22  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 49,753,658
GRCh38 10 48,545,613
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.11:g.48545613G>A
NC_000010.10:g.49753658G>A
NM_001256024.1:c.322+9850C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ARHGAP22
Accession:NM_021226
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001256025
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001256024
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001256026
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_005270014
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540013
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540006
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540015
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540002
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540003
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540011
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_011540005
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_017016476
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_017016471
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_024448100
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001347738
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001347735
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_024448099
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_024448102
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_024448106
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001347736
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NM_001347737
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425586
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425589
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425588
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425590
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425591
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425587
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425593
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425592
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425594
Location:INTRON

Gene Symbol:ARHGAP22
Accession:XM_047425595
Location:INTRON

Gene Symbol:ARHGAP22
Accession:NR_045675
Location:INTRON;NON-CODING

Gene Symbol:ARHGAP22
Accession:NR_144644
Location:INTRON;NON-CODING

Gene Symbol:ARHGAP22
Accession:NR_144646
Location:INTRON;NON-CODING

Gene Symbol:ARHGAP22
Accession:NR_144645
Location:INTRON;NON-CODING

Gene Symbol:ARHGAP22
Accession:NR_144642
Location:INTRON;NON-CODING

Gene Symbol:ARHGAP22
Accession:NR_144643
Location:INTRON;NON-CODING

Variant Samples