rs1645274452 Rat Genome Database

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Variant: rs1645274452 -  Homo sapiens

RGD ID: 38461843
RS ID: rs1645274452
ClinVar ID: CV920148
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AGO1  LOC129930123  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 36,359,773
GRCh38 1 35,894,172
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_012199.5:c.784+1G>A
NC_000001.11:g.35894172G>A
NM_012199.2:c.784+1G>A
NC_000001.10:g.36359773G>A
More... 		11/29/2019 splice donor variant uncertain significance none provided

Gene Symbol:AGO1
Accession:NM_012199
Location:INTRON

Gene Symbol:AGO1
Accession:NM_001317122
Location:INTRON

Gene Symbol:AGO1
Accession:XM_011541236
Location:INTRON

Gene Symbol:AGO1
Accession:NM_001317123
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001197640 CLINVAR
dbSNP (RS) rs1645274452 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene AGO1 CLINVAR
  LOC129930123 CLINVAR
OMIM 606228 CLINVAR