RGD:150440338 Rat Genome Database

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Variant: RGD:150440338 -  Homo sapiens

RGD ID: 150440338
RS ID: rs2713147
ClinVar ID: CV1266901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3E  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 83,047,441
GRCh38 7 83,418,125
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.13:g.83047441C>A
NM_012431.3:c.550+265G>T
LRG_1287:g.236039G>T
NG_021242.2:g.236039G>T
More... 		03/29/2019 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 RCV001690337 CLINVAR
dbSNP (RS) rs2713147 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SEMA3E CLINVAR
OMIM 608166 CLINVAR