PRAMEF12 PRAME family member 12

Information
Symbol
PRAMEF12
Type
protein-coding
Description
PRAME family member 12
Entrez Gene ID
390999
Genome
hg19
Position
chr1:12,833,881-12,838,049
Genome
hg38
Position
chr1:12,773,738-12,777,906
HGNC
HGNC:22125 HGNC
Ensembl
ENSG00000116726 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
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:22125 HGNC
Ensembl ENSG00000116726 Ensembl
AllianceGenome HGNC:22125
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000357726.5 hg38 chr1 12,773,738 12,777,906 4,169
ENST00000357726.5 hg19 chr1 12,833,881 12,838,049 4,169
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