RGD:15169951 Rat Genome Database

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Variant: RGD:15169951 -  Homo sapiens

RGD ID: 15169951
RS ID: rs752302435
ClinVar ID: CV744320
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 83,739,909
GRCh38 7 84,110,593
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006080.3:c.334-4A>G
NG_011489.1:g.89309A>G
NC_000007.14:g.84110593T>C
NC_000007.13:g.83739909T>C
More... 		12/20/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SEMA3A
Accession:XM_047419751
Location:INTRON

Gene Symbol:SEMA3A
Accession:NM_006080
Location:INTRON

Gene Symbol:SEMA3A
Accession:XM_005250110
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000905170 CLINVAR
dbSNP (RS) rs752302435 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SEMA3A CLINVAR
OMIM 603961 CLINVAR