PRAMEF5 PRAME family member 5

Information
Symbol
PRAMEF5
Type
protein-coding
Description
PRAME family member 5
Entrez Gene ID
343068
Genome
hg38
Position
chr1:13,254,198-13,263,435
HGNC
HGNC:27995 HGNC
Ensembl
ENSG00000270601 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 15
Ranking
ClinVar
0
0
0
21
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
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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 :
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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Target data :
MGeND data only
Category :
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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 PRAMEF23
SYNONYM PRAMEF5L
HGNC HGNC:27995 HGNC
Ensembl ENSG00000270601 Ensembl
AllianceGenome HGNC:27995
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000622421.3 hg38 chr1 13,254,198 13,263,435 9,238
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