INTS6 integrator complex subunit 6

Information
Symbol
INTS6
Type
protein-coding
Description
integrator complex subunit 6
Entrez Gene ID
26512
Genome
hg19
Position
chr13:51,935,713-52,027,172
Genome
hg38
Position
chr13:51,361,577-51,453,036
MIM
604331 OMIM
HGNC
HGNC:14879 HGNC
Ensembl
ENSG00000102786 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 6
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
76
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 DBI-1
SYNONYM DDX26
SYNONYM DDX26A
SYNONYM DICE1
SYNONYM HDB
SYNONYM INT6
SYNONYM Notchl2
MIM 604331 OMIM
HGNC HGNC:14879 HGNC
Ensembl ENSG00000102786 Ensembl
AllianceGenome HGNC:14879
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000311234.9 hg38 chr13 51,361,577 51,453,036 91,460
ENST00000490542.5 hg38 chr13 51,365,736 51,385,264 19,529
ENST00000398119.6 hg38 chr13 51,361,565 51,453,207 91,643
ENST00000497989.5 hg38 chr13 51,365,228 51,421,374 56,147
ENST00000442263.4 hg38 chr13 51,436,426 51,453,015 16,590
ENST00000398119.6 hg19 chr13 51,935,701 52,027,343 91,643
ENST00000311234.9 hg19 chr13 51,935,713 52,027,172 91,460
ENST00000442263.4 hg19 chr13 52,010,562 52,027,151 16,590
ENST00000490542.5 hg19 chr13 51,939,872 51,959,400 19,529
ENST00000497989.5 hg19 chr13 51,939,364 51,995,510 56,147
Genome browser