RGD:8587828 Rat Genome Database

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Variant: RGD:8587828 -  Homo sapiens

RGD ID: 8587828
ClinVar ID: CV122461
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIAPH2  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 96,459,747
GRCh38 X 97,204,748
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006729.4:c.2720-42967A>C
NG_008433.1:g.525086A>C
NC_000023.11:g.97204748A>C
NC_000023.10:g.96459747A>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:DIAPH2
Accession:NM_007309
Location:INTRON

Gene Symbol:DIAPH2
Accession:NM_006729
Location:INTRON

Variant Samples