RGD:11652110 Rat Genome Database

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Variant: RGD:11652110 -  Homo sapiens

RGD ID: 11652110
RS ID: rs886056550
ClinVar ID: CV349741
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGM6  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 2,361,610
GRCh38 20 2,380,964
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001254734.2:c.-5T>A
NG_031917.1:g.5057T>A
NC_000020.11:g.2380964T>A
NC_000020.10:g.2361610T>A
More... 		06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TGM6
Accession:NM_001254734
Location:5UTRS;EXON

Gene Symbol:TGM6
Accession:NM_198994
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000303187 CLINVAR
dbSNP (RS) rs886056550 CLINVAR
MedGen C3888031 CLINVAR
NCBI Gene TGM6 CLINVAR
OMIM 613900 CLINVAR
  613908 CLINVAR