RGD:408374949 Rat Genome Database

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Variant: RGD:408374949 -  Homo sapiens

RGD ID: 408374949
ClinVar ID: CV3508444
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3G  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 52,474,542
GRCh38 3 52,440,526
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020163.3:c.999-5G>A
NC_000003.12:g.52440526C>T
NC_000003.11:g.52474542C>T
NM_020163.2:c.999-5G>A
 03/01/2024 intron variant uncertain significance SEMA3G-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004747595 CLINVAR
NCBI Gene SEMA3G CLINVAR