RGD:150339697 Rat Genome Database

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Variant: RGD:150339697 -  Homo sapiens

RGD ID: 150339697
RS ID: rs3801479
ClinVar ID: CV1167423
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 83,014,996
GRCh38 7 83,385,680
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1287:g.268484T>C
NG_021242.2:g.268484T>C
NC_000007.14:g.83385680A>G
NC_000007.13:g.83014996A>G
More... 		08/09/2018 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 RCV001534478 CLINVAR
dbSNP (RS) rs3801479 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR