RGD:407497548 Rat Genome Database

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Variant: RGD:407497548 -  Homo sapiens

RGD ID: 407497548
ClinVar ID: CV3458660
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AOC1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 150,555,923
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001272072.2:c.1643G>A
NC_000007.14:g.150858835G>A
NC_000007.13:g.150555923G>A
NM_001091.2:c.1643G>A
More... 		06/17/2024 missense variant likely benign AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004643775 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene AOC1 CLINVAR
OMIM 104610 CLINVAR