RGD:8575199 Rat Genome Database

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Variant: RGD:8575199 -  Homo sapiens

RGD ID: 8575199
ClinVar ID: CV109544
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1E  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 181,670,259
GRCh38 1 181,701,123
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.181701123G>A
NC_000001.10:g.181670259G>A
NM_000721.3:c.1056-9831G>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CACNA1E
Accession:NM_001205293
Location:INTRON

Gene Symbol:CACNA1E
Accession:NM_000721
Location:INTRON

Gene Symbol:CACNA1E
Accession:NM_001205294
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002244
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002248
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002246
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002245
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002243
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002249
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002247
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002250
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_017002251
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_047429979
Location:INTRON

Gene Symbol:CACNA1E
Accession:XM_047429980
Location:INTRON

Variant Samples