RGD:150425593 Rat Genome Database

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Variant: RGD:150425593 -  Homo sapiens

RGD ID: 150425593
RS ID: rs111627890
ClinVar ID: CV1184019
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 83,277,587
GRCh38 7 83,648,271
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1287t1:c.115+157G>A
NM_012431.3:c.115+157G>A
LRG_1287:g.5893G>A
NG_021242.2:g.5893G>A
More... 		10/24/2018 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 RCV001558208 CLINVAR
dbSNP (RS) rs111627890 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR