RGD:8587086 Rat Genome Database

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Variant: RGD:8587086 -  Homo sapiens

RGD ID: 8587086
ClinVar ID: CV121712
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP6  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 11,507,914
GRCh38 X 11,489,794
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_013427.2:c.588+174447T>C
NG_012494.1:g.180908T>C
NC_000023.11:g.11489794A>G
NC_000023.10:g.11507914A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Gene Symbol:ARHGAP6
Accession:NM_013427
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_006125
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_001287242
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013423
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NR_109776
Location:INTRON;NON-CODING

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