RGD:10450180 Rat Genome Database

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Variant: RGD:10450180 -  Homo sapiens

RGD ID: 10450180
ClinVar ID: CV215370
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: CACNA2D1  
Reference Nucleotide: -
Variant Nucleotide: AA
Position
Assembly Chr Position
GRCh37 7 81,603,871
GRCh38 7 81,974,555
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000722.3:c.1956-4_1956-3insTT
LRG_437:g.474160_474161insTT
NG_009358.2:g.474160_474161insTT
NC_000007.14:g.81974555_81974556insAA
More... 		04/14/2015 intron variant benign AllHighlyPenetrant

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_047420820
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_001366867
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_001302890
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250574
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420819
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516571
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516570
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_006716121
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_011516572
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250572
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_005250573
Location:INTRON

Gene Symbol:CACNA2D1
Accession:NM_000722
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420822
Location:INTRON

Gene Symbol:CACNA2D1
Accession:XM_047420821
Location:INTRON

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

Variant Samples