PDCD2L programmed cell death 2 like

Information
Symbol
PDCD2L
Type
protein-coding
Description
programmed cell death 2 like
Entrez Gene ID
84306
Genome
hg19
Position
chr19:34,895,304-34,917,073
Genome
hg38
Position
chr19:34,404,399-34,426,168
MIM
615661 OMIM
HGNC
HGNC:28194 HGNC
Ensembl
ENSG00000126249 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
50
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
MIM 615661 OMIM
HGNC HGNC:28194 HGNC
Ensembl ENSG00000126249 Ensembl
AllianceGenome HGNC:28194
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000587065.2 hg38 chr19 34,404,827 34,426,168 21,342
ENST00000246535.4 hg38 chr19 34,404,399 34,426,168 21,770
ENST00000246535.4 hg19 chr19 34,895,304 34,917,073 21,770
ENST00000587065.2 hg19 chr19 34,895,732 34,917,073 21,342
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