RGD:8584529 Rat Genome Database

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Variant: RGD:8584529 -  Homo sapiens

RGD ID: 8584529
ClinVar ID: CV119102
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEGF11  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 66,327,085
GRCh38 15 66,034,747
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.66034747A>G
NC_000015.9:g.66327085A>G
NM_032445.2:c.395-52259T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MEGF11
Accession:NM_032445
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_017022670
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_017022671
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_017022674
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_017022675
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_017022673
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385030
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385031
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385028
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385032
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385033
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001385029
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001387150
Location:INTRON

Gene Symbol:MEGF11
Accession:NM_001387151
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433168
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433165
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433169
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433167
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433166
Location:INTRON

Gene Symbol:MEGF11
Accession:XM_047433170
Location:INTRON

Gene Symbol:MEGF11
Accession:NR_169555
Location:INTRON;NON-CODING

Gene Symbol:MEGF11
Accession:NR_169554
Location:INTRON;NON-CODING

Gene Symbol:MEGF11
Accession:NR_169558
Location:INTRON;NON-CODING

Gene Symbol:MEGF11
Accession:NR_169556
Location:INTRON;NON-CODING

Gene Symbol:MEGF11
Accession:NR_169557
Location:INTRON;NON-CODING

Variant Samples