POLGARF POLG alternative reading frame

Information
Symbol
POLGARF
Type
protein-coding
Description
POLG alternative reading frame
Entrez Gene ID
125316803
Genome
hg19
Position
chr15:89,873,439-89,877,040
Genome
hg38
Position
chr15:89,330,208-89,333,809
MIM
620759 OMIM
HGNC
HGNC:56246 HGNC
Ensembl
ENSG00000291307 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 56
Likely pathogenic 1 40
Benign 0 30
Likely benign 0 348
Conflicting classifications of pathogenicity 0 80
Uncertain significance 0 522
Ranking
ClinVar
0
4
212
738
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM ORF-Y
SYNONYM POLG
MIM 620759 OMIM
HGNC HGNC:56246 HGNC
Ensembl ENSG00000291307 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000706918.1 hg38 chr15 89,330,208 89,333,809 3,602
ENST00000706918.1 hg19 chr15 89,873,439 89,877,040 3,602
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