rs77944127 Rat Genome Database

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Variant: rs77944127 -  Homo sapiens

RGD ID: 150414323
RS ID: rs77944127
ClinVar ID: CV1176335
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  LARS2-AS1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 45,526,966
GRCh38 3 45,485,474
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1353t1:c.1019-218T>A
NC_000003.11:g.45526966T>A
NM_001368263.1:c.1019-218T>A
NM_015340.4:c.1019-218T>A
More... 		01/06/2019 intron variant likely benign none provided

Gene Symbol:LARS2
Accession:XM_011533554
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447829
Location:INTRON

Gene Symbol:LARS2
Accession:NM_001368263
Location:INTRON

Gene Symbol:LARS2
Accession:NM_015340
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447830
Location:INTRON

Gene Symbol:LARS2
Accession:XM_017006042
Location:INTRON

Gene Symbol:LARS2-AS1
Accession:NR_048543
Location:INTRON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001548077 CLINVAR
dbSNP (RS) rs77944127 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LARS2 CLINVAR
  LARS2-AS1 CLINVAR
OMIM 604544 CLINVAR