RGD:150481048 Rat Genome Database

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Variant: RGD:150481048 -  Homo sapiens

RGD ID: 150481048
RS ID: rs2709926
ClinVar ID: CV1239704
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 83,029,742
GRCh38 7 83,400,426
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1287t1:c.1144-176C>A
NM_012431.3:c.1144-176C>A
NM_001178129.2:c.964-176C>A
LRG_1287:g.253738C>A
More... 		10/17/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEMA3E
Accession:NM_012431
Location:INTRON

Gene Symbol:SEMA3E
Accession:NM_001178129
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652867 CLINVAR
dbSNP (RS) rs2709926 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR