RGD:408386835 Rat Genome Database

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Variant: RGD:408386835 -  Homo sapiens

RGD ID: 408386835
ClinVar ID: CV3524253
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 45,515,751
GRCh38 3 45,474,259
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1353t1:c.767T>C
NM_001368263.1:c.767T>C
NM_015340.4:c.767T>C
LRG_1353:g.90696T>C
More... 		12/05/2023 missense variant uncertain significance none provided

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Database
Acc Id
Source(s)
ClinVar RCV004768127 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LARS2 CLINVAR
OMIM 604544 CLINVAR