rs74067514 Rat Genome Database

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Variant: rs74067514 -  Homo sapiens

RGD ID: 150421210
RS ID: rs74067514
ClinVar ID: CV1196609
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YARS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 33,246,165
GRCh38 1 32,780,564
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003680.4:c.1141-286G>A
LRG_273:g.42469G>A
NG_008408.1:g.42469G>A
NC_000001.11:g.32780564C>T
More... 		10/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:YARS1
Accession:NM_003680
Location:INTRON

Gene Symbol:YARS1
Accession:XM_011542347
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001577939 CLINVAR
dbSNP (RS) rs74067514 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene YARS1 CLINVAR
OMIM 603623 CLINVAR