rs184249741 Rat Genome Database

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Variant: rs184249741 -  Homo sapiens

RGD ID: 11593814
RS ID: rs184249741
ClinVar ID: CV282094
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YARS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 33,241,143
GRCh38 1 32,775,542
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_273t1:c.*439T>C
LRG_273:g.47491T>C
NG_008408.1:g.47491T>C
NC_000001.11:g.32775542A>G
More... 		01/12/2018 3 prime utr variant benign|uncertain significance CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE C
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:YARS1
Accession:NM_003680
Location:3UTRS;EXON

Gene Symbol:YARS1
Accession:XM_011542347
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000352414 CLINVAR
dbSNP (RS) rs184249741 CLINVAR
MedGen C1842237 CLINVAR
NCBI Gene YARS CLINVAR
OMIM 603623 CLINVAR
  608323 CLINVAR