RGD:597755765 Rat Genome Database

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Variant: RGD:597755765 -  Homo sapiens

RGD ID: 597755765
ClinVar ID: CV3603576
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127400453  SOD3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 24,801,382
GRCh38 4 24,799,760
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003102.4:c.239G>C
NG_102416.1:g.136G>C
NG_012213.2:g.9189G>C
NG_012213.1:g.9298G>C
More... 		10/28/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004868258 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SOD3 CLINVAR
OMIM 185490 CLINVAR