RGD:8586290 Rat Genome Database

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Variant: RGD:8586290 -  Homo sapiens

RGD ID: 8586290
ClinVar ID: CV120889
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MACROD2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 15,476,485
GRCh38 20 15,495,840
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.11:g.15495840C>T
NC_000020.10:g.15476485C>T
NM_001033087.1:c.-134-3934C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MACROD2
Accession:NM_001351664
Location:5UTRS;INTRON

Gene Symbol:MACROD2
Accession:NM_001033087
Location:5UTRS;INTRON

Gene Symbol:MACROD2
Accession:NM_080676
Location:INTRON

Gene Symbol:MACROD2
Accession:NM_001351661
Location:INTRON

Gene Symbol:MACROD2
Accession:XM_024451834
Location:INTRON

Gene Symbol:MACROD2
Accession:NM_001351663
Location:INTRON

Gene Symbol:MACROD2
Accession:XM_017027675
Location:INTRON

Gene Symbol:MACROD2
Accession:XM_017027676
Location:INTRON

Variant Samples