ATP6V1G2-DDX39B ATP6V1G2-DDX39B readthrough (NMD candidate)

Information
Symbol
ATP6V1G2-DDX39B
Type
ncRNA
Description
ATP6V1G2-DDX39B readthrough (NMD candidate)
Entrez Gene ID
100532737
Genome
hg19
Position
chr6:31,497,996-31,514,359
Genome
hg38
Position
chr6:31,530,219-31,546,582
HGNC
HGNC:41999 HGNC
Ensembl
ENSG00000254870 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
not provided 24 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
42
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
HGNC HGNC:41999 HGNC
Ensembl ENSG00000254870 Ensembl
AllianceGenome HGNC:41999
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376185.5 hg38 chr6 31,530,219 31,546,582 16,364
ENST00000376185.5 hg19 chr6 31,497,996 31,514,359 16,364
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