RGD:11646364 Rat Genome Database

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Variant: RGD:11646364 -  Homo sapiens

RGD ID: 11646364
RS ID: rs886048744
ClinVar ID: CV329772
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TYR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 88,911,081
GRCh38 11 89,177,913
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008748.1:g.5042A>G
NC_000011.10:g.89177913A>G
NC_000011.9:g.88911081A>G
NM_000372.5:c.-41A>G
More...
06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TYR
Accession:NM_000372
Location:5UTRS;EXON

Gene Symbol:TYR
Accession:XM_011542970
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000270512 CLINVAR
dbSNP (RS) rs886048744 CLINVAR
MedGen C0078918 CLINVAR
NCBI Gene TYR CLINVAR
OMIM 606933 CLINVAR
SNOMED CT 63844009 CLINVAR