RGD:150462353 Rat Genome Database

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Variant: RGD:150462353 -  Homo sapiens

RGD ID: 150462353
RS ID: rs3801506
ClinVar ID: CV1264724
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 83,047,883
GRCh38 7 83,418,567
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001178129.2:c.277-84C>T
NM_012431.3:c.457-84C>T
LRG_1287:g.235597C>T
NG_021242.2:g.235597C>T
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 RCV001682348 CLINVAR
dbSNP (RS) rs3801506 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR