RGD:8649476 Rat Genome Database

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Variant: RGD:8649476 -  Homo sapiens

RGD ID: 8649476
ClinVar ID: CV126050
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 83,216,273
GRCh38 7 83,586,957
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012431.2:c.115+61471C>G
NG_021242.1:g.67207C>G
NC_000007.14:g.83586957G>C
NC_000007.13:g.83216273G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SEMA3E
Accession:NM_001178129
Location:5UTRS;INTRON

Gene Symbol:SEMA3E
Accession:NM_012431
Location:INTRON

Variant Samples