PRAMEF17 PRAME family member 17

Information
Symbol
PRAMEF17
Type
protein-coding
Description
PRAME family member 17
Entrez Gene ID
391004
Genome
hg19
Position
chr1:13,716,092-13,719,089
Genome
hg38
Position
chr1:13,389,632-13,392,629
HGNC
HGNC:29485 HGNC
Ensembl
ENSG00000204479 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
66
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:29485 HGNC
Ensembl ENSG00000204479 Ensembl
AllianceGenome HGNC:29485
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376098.4 hg38 chr1 13,389,632 13,392,629 2,998
ENST00000376098.4 hg19 chr1 13,716,092 13,719,089 2,998
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