RGD:156382821 Rat Genome Database

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Variant: RGD:156382821 -  Homo sapiens

RGD ID: 156382821
ClinVar ID: CV1960991
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 45,459,078
GRCh38 3 45,417,586
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1353t1:c.455+13A>G
NM_001368263.1:c.455+13A>G
NM_015340.4:c.455+13A>G
LRG_1353:g.34023A>G
More... 		06/23/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:LARS2
Accession:XM_047447830
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447829
Location:INTRON

Gene Symbol:LARS2
Accession:NM_015340
Location:INTRON

Gene Symbol:LARS2
Accession:XM_011533554
Location:INTRON

Gene Symbol:LARS2
Accession:NM_001368263
Location:INTRON

Gene Symbol:LARS2
Accession:XM_017006042
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002583292 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LARS2 CLINVAR
OMIM 604544 CLINVAR