RGD:150492182 Rat Genome Database

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Variant: RGD:150492182 -  Homo sapiens

RGD ID: 150492182
RS ID: rs330570
ClinVar ID: CV1280874
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CARS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 13 111,293,847
GRCh38 13 110,641,500
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000013.11:g.110641500G>A
NM_001352252.2:c.*37C>T
NM_024537.4:c.*37C>T
NG_042045.2:g.77102C>T
More... 		06/26/2018 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CARS2
Accession:XM_047430609
Location:3UTRS;EXON

Gene Symbol:CARS2
Accession:NM_001352252
Location:3UTRS;EXON

Gene Symbol:CARS2
Accession:XM_006719953
Location:3UTRS;EXON

Gene Symbol:CARS2
Accession:XM_047430606
Location:3UTRS;EXON

Gene Symbol:CARS2
Accession:NM_024537
Location:3UTRS;EXON

Gene Symbol:CARS2
Accession:NR_147941
Location:EXON;NON-CODING

Gene Symbol:CARS2
Accession:NR_147942
Location:EXON;NON-CODING

Gene Symbol:CARS2
Accession:NM_001352253
Location:INTRON

Gene Symbol:CARS2
Accession:XM_011521118
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430605
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430608
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430607
Location:INTRON

Gene Symbol:CARS2
Accession:XM_017020742
Location:INTRON

Gene Symbol:CARS2
Accession:XR_001749667
Location:INTRON;NON-CODING

Gene Symbol:CARS2
Accession:XR_007063696
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001716763 CLINVAR
dbSNP (RS) rs330570 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CARS2 CLINVAR
OMIM 612800 CLINVAR