RGD:11658911 Rat Genome Database

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Variant: RGD:11658911 -  Homo sapiens

RGD ID: 11658911
RS ID: rs886056623
ClinVar ID: CV349873
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNMT3B  LOC127893039  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 31,396,286
GRCh38 20 32,808,480
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NM_001207055.2:c.*577C>T
NM_001207056.2:c.*577C>T
NM_006892.3:c.*577C>T
LRG_56t1:c.*577C>T
More... 		06/14/2016 3 prime utr variant uncertain significance childhood <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:DNMT3B
Accession:XM_047439956
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424353
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:XM_047439950
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424357
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:XM_047439955
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001207055
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424351
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424356
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424354
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424359
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_175849
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:XM_047439946
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001207056
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424355
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424358
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424352
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_001424360
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_175848
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_006892
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:NM_175850
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:XM_047439949
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:DNMT3B
Accession:XM_047439959
Location:INTRON

Gene Symbol:DNMT3B
Accession:XM_047439960
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000353066 CLINVAR
dbSNP (RS) rs886056623 CLINVAR
MedGen C4551557 CLINVAR
NCBI Gene DNMT3B CLINVAR
OMIM 242860 CLINVAR
  602900 CLINVAR