RGD:408391815 Rat Genome Database

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Variant: RGD:408391815 -  Homo sapiens

RGD ID: 408391815
ClinVar ID: CV3523437
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AGO1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 36,383,246
GRCh38 1 35,917,645
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001317123.2:c.1856A>C
NM_001317122.2:c.2081A>C
NM_012199.5:c.2081A>C
NC_000001.11:g.35917645A>C
More... 		11/09/2023 missense variant uncertain significance none provided

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Database
Acc Id
Source(s)
ClinVar RCV004770811 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AGO1 CLINVAR
OMIM 606228 CLINVAR