RGD:11659432 Rat Genome Database

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Variant: RGD:11659432 -  Homo sapiens

RGD ID: 11659432
RS ID: rs886061482
ClinVar ID: CV307847
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AARS2  POLR1C  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 44,267,032
GRCh38 6 44,299,295
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020745.4:c.*1252A>C
NG_031952.1:g.19032A>C
NC_000006.12:g.44299295T>G
NC_000006.11:g.44267032T>G
More... 		06/14/2016 3 prime utr variant uncertain significance CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE; Combined oxidative phosphorylation deficiency 8
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:AARS2
Accession:NM_020745
Location:3UTRS;EXON

Gene Symbol:AARS2
Accession:XM_005249245
Location:3UTRS;EXON

Gene Symbol:POLR1C
Accession:NM_001318876
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_203290
Location:INTRON

Gene Symbol:POLR1C
Accession:XM_047419577
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_001363658
Location:INTRON

Gene Symbol:AARS2
Accession:XR_007059282
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000357920 CLINVAR
dbSNP (RS) rs886061482 CLINVAR
MedGen C4518839 CLINVAR
NCBI Gene AARS2 CLINVAR
  POLR1C CLINVAR
OMIM 610060 CLINVAR
  612035 CLINVAR
  614096 CLINVAR