RGD:8587252 Rat Genome Database

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Variant: RGD:8587252 -  Homo sapiens

RGD ID: 8587252
ClinVar ID: CV121879
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAGEC3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 140,948,026
GRCh38 X 141,860,240
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_138702.1:c.124-5231C>T
NG_013272.1:g.26925C>T
NC_000023.11:g.141860240C>T
NC_000023.10:g.140948026C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MAGEC3
Accession:XM_011531267
Location:INTRON

Gene Symbol:MAGEC3
Accession:NM_177456
Location:INTRON

Gene Symbol:MAGEC3
Accession:NM_138702
Location:INTRON

Variant Samples