RGD:14736526 Rat Genome Database

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Variant: RGD:14736526 -  Homo sapiens

RGD ID: 14736526
RS ID: rs10423673
ClinVar ID: CV669895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNMT1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 10,244,531
GRCh38 19 10,133,855
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001318731.2:c.4502-154G>A
NM_001379.4:c.4817-154G>A
NM_001318730.2:c.4826-154G>A
NM_001130823.3:c.4865-154G>A
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNMT1
Accession:NM_001318731
Location:INTRON

Gene Symbol:DNMT1
Accession:NM_001379
Location:INTRON

Gene Symbol:DNMT1
Accession:NM_001130823
Location:INTRON

Gene Symbol:DNMT1
Accession:NM_001318730
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838513 CLINVAR
dbSNP (RS) rs10423673 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNMT1 CLINVAR
OMIM 126375 CLINVAR