rs72963007 Rat Genome Database

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Variant: rs72963007 -  Homo sapiens

RGD ID: 15195517
RS ID: rs72963007
ClinVar ID: CV730251
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TET2  TET2-AS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 106,164,723
GRCh38 4 105,243,566
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001127208.2:c.3595-4G>A
NM_001127208.3:c.3595-4G>A
NC_000004.11:g.106164723G>A
NG_028191.1:g.102692G>A
More... 		01/19/2024 intron variant benign|likely benign none provided; TET2-related condition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TET2
Accession:NM_001127208
Location:INTRON

Gene Symbol:TET2
Accession:XM_005263082
Location:INTRON

Gene Symbol:TET2
Accession:XM_047415840
Location:INTRON

Gene Symbol:TET2
Accession:XM_024454103
Location:INTRON

Gene Symbol:TET2
Accession:XM_047415841
Location:INTRON

Gene Symbol:TET2
Accession:XM_047415839
Location:INTRON

Gene Symbol:TET2
Accession:XM_047415843
Location:INTRON

Gene Symbol:TET2
Accession:XM_017008319
Location:INTRON

Gene Symbol:TET2
Accession:XM_006714242
Location:INTRON

Gene Symbol:TET2
Accession:XM_024454102
Location:INTRON

Gene Symbol:TET2
Accession:NM_017628
Location:INTRON

Gene Symbol:TET2
Accession:XM_047415842
Location:INTRON

Gene Symbol:TET2
Accession:XR_007057933
Location:INTRON;NON-CODING

Gene Symbol:TET2-AS1
Accession:NR_126420
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000889525 CLINVAR
  RCV003910547 CLINVAR
dbSNP (RS) rs72963007 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TET2 CLINVAR
  TET2-AS1 CLINVAR
OMIM 612839 CLINVAR