PRAMEF18 PRAME family member 18

Information
Symbol
PRAMEF18
Type
protein-coding
Description
PRAME family member 18
Entrez Gene ID
391003
Genome
hg38
Position
chr1:13,222,695-13,226,154
HGNC
HGNC:30693 HGNC
Ensembl
ENSG00000279804 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 1
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
37
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
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:30693 HGNC
Ensembl ENSG00000279804 Ensembl
AllianceGenome HGNC:30693
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000624297.3 hg38 chr1 13,222,695 13,226,154 3,460
Genome browser