PPFIA2-AS1 PPFIA2 antisense RNA 1

Information
Symbol
PPFIA2-AS1
Type
ncRNA
Description
PPFIA2 antisense RNA 1
Entrez Gene ID
102724663
Genome
hg19
Position
chr12:81,664,454-81,706,090
Genome
hg38
Position
chr12:81,270,675-81,312,311
HGNC
HGNC:53397 HGNC
Ensembl
ENSG00000257467 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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
HGNC HGNC:53397 HGNC
Ensembl ENSG00000257467 Ensembl
AllianceGenome HGNC:53397
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000654866.1 hg38 chr12 81,270,669 81,312,110 41,442
ENST00000552534.5 hg38 chr12 81,279,185 81,312,373 33,189
ENST00000553197.5 hg38 chr12 81,279,201 81,312,289 33,089
ENST00000549161.5 hg38 chr12 81,270,675 81,312,311 41,637
ENST00000654866.1 hg19 chr12 81,664,448 81,705,889 41,442
ENST00000549161.5 hg19 chr12 81,664,454 81,706,090 41,637
ENST00000552534.5 hg19 chr12 81,672,964 81,706,152 33,189
ENST00000553197.5 hg19 chr12 81,672,980 81,706,068 33,089
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