PRAMEF9 PRAME family member 9

Information
Symbol
PRAMEF9
Type
protein-coding
Description
PRAME family member 9
Entrez Gene ID
343070
Genome
hg38
Position
chr1:13,171,848-13,179,459
HGNC
HGNC:27996 HGNC
Ensembl
ENSG00000204505 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
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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:27996 HGNC
Ensembl ENSG00000204505 Ensembl
AllianceGenome HGNC:27996
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000415919.3 hg38 chr1 13,171,848 13,179,459 7,612
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