RGD:408373872 Rat Genome Database

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Variant: RGD:408373872 -  Homo sapiens

RGD ID: 408373872
ClinVar ID: CV3512996
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SEMA3G  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 52,473,977
GRCh38 3 52,439,961
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020163.3:c.1281T>C
NC_000003.12:g.52439961A>G
NC_000003.11:g.52473977A>G
NM_020163.2:c.1281T>C
More... 		08/01/2022 synonymous variant likely benign SEMA3G-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004745769 CLINVAR
NCBI Gene SEMA3G CLINVAR