PRAMEF13 PRAME family member 13

Information
Symbol
PRAMEF13
Type
protein-coding
Description
PRAME family member 13
Entrez Gene ID
400736
Genome
hg19
Position
chr1:13,447,429-13,452,656
Genome
hg38
Position
chr1:13,196,188-13,201,409
HGNC
HGNC:13262 HGNC
Ensembl
ENSG00000279169 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 :
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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:13262 HGNC
Ensembl ENSG00000279169 Ensembl
AllianceGenome HGNC:13262
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000625019.3 hg38 chr1 13,196,188 13,201,409 5,222
ENST00000638454.1 hg38 chr1 13,196,330 13,198,130 1,801
ENST00000625019.3 hg19 chr1 13,447,429 13,452,656 5,228
ENST00000638454.1 hg19 chr1 13,447,556 13,449,333 1,778
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