RGD:155266881 Rat Genome Database

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Variant: RGD:155266881 -  Homo sapiens

RGD ID: 155266881
ClinVar ID: CV1704169
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POLH  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 43,578,461
GRCh38 6 43,610,724
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001291970.2:c.1244+1G>T
NM_001291969.2:c.872+1G>T
LRG_470:g.39584G>T
NG_009252.1:g.39584G>T
More... 		intron variant|splice donor variant not provided none provided

Gene Symbol:POLH
Accession:NM_006502
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_203290
Location:INTRON

Gene Symbol:POLH
Accession:NM_001291970
Location:INTRON

Gene Symbol:POLH
Accession:NM_001291969
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_001318876
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_001363658
Location:INTRON

Gene Symbol:POLH
Accession:XM_047418900
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV002284156 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene POLH CLINVAR
OMIM 603968 CLINVAR