RGD:150475322 Rat Genome Database

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Variant: RGD:150475322 -  Homo sapiens

RGD ID: 150475322
RS ID: rs302114
ClinVar ID: CV1217931
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 83,278,227
GRCh38 7 83,648,911
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.83648911C>A
NC_000007.13:g.83278227C>A
LRG_1287t1:c.-369G>T
NM_012431.3:c.-369G>T
More... 		08/08/2019 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEMA3E
Accession:NM_012431
Location:5UTRS;EXON

Gene Symbol:SEMA3E
Accession:NM_001178129
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001615942 CLINVAR
dbSNP (RS) rs302114 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR