RGD:8587082 Rat Genome Database

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Variant: RGD:8587082 -  Homo sapiens

RGD ID: 8587082
ClinVar ID: CV121708
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP6  LOC124905246  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 11,451,400
GRCh38 X 11,433,280
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_013427.2:c.589-178573C>T
NG_012494.1:g.237422C>T
NC_000023.11:g.11433280G>A
NC_000023.10:g.11451400G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Gene Symbol:LOC124905246
Accession:XR_007068392
Location:EXON;NON-CODING

Gene Symbol:ARHGAP6
Accession:NM_006125
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_001287242
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013427
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013423
Location:INTRON

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

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