RGD:150415440 Rat Genome Database

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Variant: RGD:150415440 -  Homo sapiens

RGD ID: 150415440
RS ID: rs113176536
ClinVar ID: CV1190705
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 82,997,628
GRCh38 7 83,368,312
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.83368312G>A
NC_000007.13:g.82997628G>A
LRG_1287t1:c.1876-274C>T
NM_001178129.2:c.1696-274C>T
More... 		03/31/2019 intron variant likely 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 RCV001567986 CLINVAR
dbSNP (RS) rs113176536 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR