C19orf38 chromosome 19 open reading frame 38

Information
Symbol
C19orf38
Type
protein-coding
Description
chromosome 19 open reading frame 38
Entrez Gene ID
255809
Genome
hg19
Position
chr19:10,959,091-10,980,466
Genome
hg38
Position
chr19:10,848,415-10,869,790
HGNC
HGNC:34073 HGNC
Ensembl
ENSG00000214212 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Ranking
ClinVar
0
0
0
2
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
SYNONYM HIDE1
HGNC HGNC:34073 HGNC
Ensembl ENSG00000214212 Ensembl
AllianceGenome HGNC:34073
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000592854.5 hg38 chr19 10,836,575 10,869,470 32,896
ENST00000397820.5 hg38 chr19 10,848,415 10,869,790 21,376
ENST00000592854.5 hg19 chr19 10,947,251 10,980,146 32,896
ENST00000397820.5 hg19 chr19 10,959,091 10,980,466 21,376
Genome browser