RGD:150495395 Rat Genome Database

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Variant: RGD:150495395 -  Homo sapiens

RGD ID: 150495395
RS ID: rs148358273
ClinVar ID: CV1204996
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CARS2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 13 111,294,603
GRCh38 13 110,642,256
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024537.4:c.1623+59G>A
NM_001352252.2:c.837+59G>A
NG_042045.2:g.76346G>A
NC_000013.11:g.110642256C>T
More... 		09/26/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CARS2
Accession:XM_047430609
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430605
Location:INTRON

Gene Symbol:CARS2
Accession:NM_001352252
Location:INTRON

Gene Symbol:CARS2
Accession:NM_001352253
Location:INTRON

Gene Symbol:CARS2
Accession:XM_017020742
Location:INTRON

Gene Symbol:CARS2
Accession:NM_024537
Location:INTRON

Gene Symbol:CARS2
Accession:XM_011521118
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430608
Location:INTRON

Gene Symbol:CARS2
Accession:XM_006719953
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430607
Location:INTRON

Gene Symbol:CARS2
Accession:XM_047430606
Location:INTRON

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

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001593488 CLINVAR
dbSNP (RS) rs148358273 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CARS2 CLINVAR
OMIM 612800 CLINVAR