PHF19 PHD finger protein 19

Information
Symbol
PHF19
Type
protein-coding
Description
PHD finger protein 19
Entrez Gene ID
26147
Genome
hg19
Position
chr9:123,617,976-123,657,174
Genome
hg38
Position
chr9:120,855,698-120,894,896
MIM
609740 OMIM
HGNC
HGNC:24566 HGNC
Ensembl
ENSG00000119403 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 0
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
38
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
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
SYNONYM MTF2L1
SYNONYM PCL3
SYNONYM TDRD19B
MIM 609740 OMIM
HGNC HGNC:24566 HGNC
Ensembl ENSG00000119403 Ensembl
AllianceGenome HGNC:24566
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000312189.10 hg38 chr9 120,869,587 120,877,188 7,602
ENST00000373896.8 hg38 chr9 120,855,651 120,877,188 21,538
ENST00000616568.5 hg38 chr9 120,855,698 120,894,896 39,199
ENST00000419155.5 hg38 chr9 120,855,652 120,868,911 13,260
ENST00000373896.8 hg19 chr9 123,617,929 123,639,466 21,538
ENST00000419155.5 hg19 chr9 123,617,930 123,631,189 13,260
ENST00000616568.5 hg19 chr9 123,617,976 123,657,174 39,199
ENST00000312189.10 hg19 chr9 123,631,865 123,639,466 7,602
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