RGD:8582190 Rat Genome Database

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Variant: RGD:8582190 -  Homo sapiens

RGD ID: 8582190
ClinVar ID: CV116659
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEI4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 78,492,144
GRCh38 6 77,782,427
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.77782427T>C
NC_000006.11:g.78492144T>C
NM_001282136.1:c.768+20762T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MEI4
Accession:NM_001282136
Location:INTRON

Gene Symbol:MEI4
Accession:XM_005248774
Location:INTRON

Gene Symbol:MEI4
Accession:NM_001322247
Location:INTRON

Gene Symbol:MEI4
Accession:XM_017010155
Location:INTRON

Variant Samples