RGD:8649456 Rat Genome Database

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Variant: RGD:8649456 -  Homo sapiens

RGD ID: 8649456
ClinVar ID: CV126030
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA2D1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 81,681,242
GRCh38 7 82,051,926
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_437t1:c.879+8502G>C
LRG_437:g.396790G>C
NG_009358.2:g.396790G>C
NC_000007.14:g.82051926C>G
More... 		intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CACNA2D1
Accession:XM_006716118
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_006716120
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516570
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420822
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_006716121
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420820
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420819
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_001366867
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250572
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516571
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_001302890
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_000722
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250573
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250574
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516572
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420821
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XR_001744873
Location:INTRON;NON-CODING

Variant Samples