RGD:8586823 Rat Genome Database

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Variant: RGD:8586823 -  Homo sapiens

RGD ID: 8586823
ClinVar ID: CV121446
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CECR2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 18,001,574
GRCh38 22 17,522,546
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290046.1:c.466-1572A>T
NG_033989.1:g.167598A>T
NC_000022.11:g.17522546A>T
NC_000022.10:g.18001574A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CECR2
Accession:NM_001290046
Location:INTRON

Gene Symbol:CECR2
Accession:XM_047441342
Location:INTRON

Gene Symbol:CECR2
Accession:XM_011546128
Location:INTRON

Gene Symbol:CECR2
Accession:XM_024452234
Location:INTRON

Gene Symbol:CECR2
Accession:XM_047441341
Location:INTRON

Gene Symbol:CECR2
Accession:XM_017028785
Location:INTRON

Gene Symbol:CECR2
Accession:XM_006724079
Location:INTRON

Gene Symbol:CECR2
Accession:XM_011546132
Location:INTRON

Gene Symbol:CECR2
Accession:XM_011546129
Location:INTRON

Gene Symbol:CECR2
Accession:XM_047441343
Location:INTRON

Gene Symbol:CECR2
Accession:NM_001290047
Location:INTRON

Gene Symbol:CECR2
Accession:XM_047441344
Location:INTRON

Gene Symbol:CECR2
Accession:XM_047441345
Location:INTRON

Variant Samples