RGD:408379111 Rat Genome Database

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Variant: RGD:408379111 -  Homo sapiens

RGD ID: 408379111
ClinVar ID: CV3516099
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: AGO1  
Reference Nucleotide: -
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 36,354,045
GRCh38 1 35,888,444
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001317123.2:c.-177dup
NM_001317122.2:c.49dup
NM_012199.5:c.49dup
NC_000001.11:g.35888450dup
More... 		04/09/2024 5 prime utr variant uncertain significance AGO1-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004752590 CLINVAR
NCBI Gene AGO1 CLINVAR
OMIM 606228 CLINVAR