C19orf44 chromosome 19 open reading frame 44

Information
Symbol
C19orf44
Type
protein-coding
Description
chromosome 19 open reading frame 44
Entrez Gene ID
84167
Genome
hg19
Position
chr19:16,607,205-16,632,163
Genome
hg38
Position
chr19:16,496,394-16,521,352
HGNC
HGNC:26141 HGNC
Ensembl
ENSG00000105072 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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:26141 HGNC
Ensembl ENSG00000105072 Ensembl
AllianceGenome HGNC:26141
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000221671.8 hg38 chr19 16,496,394 16,521,352 24,959
ENST00000594035.5 hg38 chr19 16,496,394 16,518,619 22,226
ENST00000594035.5 hg19 chr19 16,607,205 16,629,430 22,226
ENST00000221671.8 hg19 chr19 16,607,205 16,632,163 24,959
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