RGD:408378710 Rat Genome Database

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Variant: RGD:408378710 -  Homo sapiens

RGD ID: 408378710
ClinVar ID: CV3505370
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3G  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 52,475,291
GRCh38 3 52,441,275
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020163.3:c.802C>G
NC_000003.12:g.52441275G>C
NC_000003.11:g.52475291G>C
NM_020163.2:c.802C>G
More... 		05/15/2024 missense variant uncertain significance SEMA3G-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004728043 CLINVAR
NCBI Gene SEMA3G CLINVAR