RGD:150492421 Rat Genome Database

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Variant: RGD:150492421 -  Homo sapiens

RGD ID: 150492421
RS ID: rs3801661
ClinVar ID: CV1225470
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 82,996,706
GRCh38 7 83,367,390
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1287t1:c.*196T>A
NM_001178129.2:c.*196T>A
NM_012431.3:c.*196T>A
LRG_1287:g.286774T>A
More... 		08/09/2018 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEMA3E
Accession:NM_012431
Location:3UTRS;EXON

Gene Symbol:SEMA3E
Accession:NM_001178129
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001618985 CLINVAR
dbSNP (RS) rs3801661 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR