rs1553625369 Rat Genome Database

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Variant: rs1553625369 -  Homo sapiens

RGD ID: 13541262
RS ID: rs1553625369
ClinVar ID: CV500274
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 45,430,157
GRCh38 3 45,388,665
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_033907.1:g.5083C>G
NC_000003.12:g.45388665C>G
NC_000003.11:g.45430157C>G
NM_015340.4:c.-103C>G
More... 		05/15/2017 5 prime utr variant likely benign AllHighlyPenetrant

Gene Symbol:LARS2
Accession:NM_015340
Location:5UTRS;EXON

Gene Symbol:LARS2
Accession:XM_011533554
Location:5UTRS;EXON

Gene Symbol:LARS2
Accession:XM_047447830
Location:5UTRS;EXON

Gene Symbol:LARS2
Accession:NM_001368263
Location:5UTRS;EXON

Gene Symbol:LARS2
Accession:XM_017006042
Location:5UTRS;EXON

Gene Symbol:LARS2
Accession:XM_047447829
Location:5UTRS;EXON

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Database
Acc Id
Source(s)
ClinVar RCV000615917 CLINVAR
dbSNP (RS) rs1553625369 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LARS2 CLINVAR
OMIM 604544 CLINVAR