rs111651315 Rat Genome Database

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Variant: rs111651315 -  Homo sapiens

RGD ID: 150415049
RS ID: rs111651315
ClinVar ID: CV1196610
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YARS1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 33,247,751
GRCh38 1 32,782,150
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.1042+254C>G
LRG_273:g.40883C>G
NG_008408.1:g.40883C>G
NC_000001.11:g.32782150G>C
More... 		03/11/2019 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 RCV001575226 CLINVAR
dbSNP (RS) rs111651315 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene YARS1 CLINVAR
OMIM 603623 CLINVAR