R3HDM4 R3H domain containing 4

Information
Symbol
R3HDM4
Type
protein-coding
Description
R3H domain containing 4
Entrez Gene ID
91300
Genome
hg19
Position
chr19:896,503-913,219
Genome
hg38
Position
chr19:896,503-913,219
HGNC
HGNC:28270 HGNC
Ensembl
ENSG00000198858 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
40
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 :
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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 C19orf22
HGNC HGNC:28270 HGNC
Ensembl ENSG00000198858 Ensembl
AllianceGenome HGNC:28270
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000626716.1 hg38 chr19 902,561 913,157 10,597
ENST00000361574.10 hg38 chr19 896,503 913,219 16,717
ENST00000587975.2 hg38 chr19 896,504 913,245 16,742
ENST00000361574.10 hg19 chr19 896,503 913,219 16,717
ENST00000587975.2 hg19 chr19 896,504 913,245 16,742
ENST00000626716.1 hg19 chr19 902,561 913,157 10,597
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