PRAMEF11 PRAME family member 11

Information
Symbol
PRAMEF11
Type
protein-coding
Description
PRAME family member 11
Entrez Gene ID
440560
Genome
hg19
Position
chr1:13,052,394-13,052,998
Genome
hg38
Position
chr1:12,824,605-12,831,410
HGNC
HGNC:14086 HGNC
Ensembl
ENSG00000239810 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 11
Uncertain significance 0 35
Ranking
ClinVar
0
0
0
46
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 :
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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:14086 HGNC
Ensembl ENSG00000239810 Ensembl
AllianceGenome HGNC:14086
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000619922.1 hg38 chr1 12,824,605 12,831,410 6,806
ENST00000436041.1 hg19 chr1 13,052,394 13,052,998 605
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