RGD:408381587 Rat Genome Database

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Variant: RGD:408381587 -  Homo sapiens

RGD ID: 408381587
ClinVar ID: CV3501968
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IQCE  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 2,625,834
GRCh38 7 2,586,200
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001287501.2:c.630-8T>G
NM_001287502.2:c.630-8T>G
NM_001287500.2:c.777-8T>G
NM_001410865.1:c.777-8T>G
More... 		12/05/2022 intron variant uncertain significance none provided

Gene Symbol:IQCE
Accession:XM_017011902
Location:INTRON

Gene Symbol:IQCE
Accession:XM_047420081
Location:INTRON

Gene Symbol:IQCE
Accession:NM_001287499
Location:INTRON

Gene Symbol:IQCE
Accession:NM_001287501
Location:INTRON

Gene Symbol:IQCE
Accession:NM_001287500
Location:INTRON

Gene Symbol:IQCE
Accession:XM_017011903
Location:INTRON

Gene Symbol:IQCE
Accession:XM_006715676
Location:INTRON

Gene Symbol:IQCE
Accession:XM_024446699
Location:INTRON

Gene Symbol:IQCE
Accession:NM_001287502
Location:INTRON

Gene Symbol:IQCE
Accession:XM_047420083
Location:INTRON

Gene Symbol:IQCE
Accession:NM_152558
Location:INTRON

Gene Symbol:IQCE
Accession:XM_011515244
Location:INTRON

Gene Symbol:IQCE
Accession:XM_047420084
Location:INTRON

Gene Symbol:IQCE
Accession:NM_001410865
Location:INTRON

Gene Symbol:IQCE
Accession:XM_011515242
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV004729496 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IQCE CLINVAR
OMIM 617631 CLINVAR