INTS2 integrator complex subunit 2

Information
Symbol
INTS2
Type
protein-coding
Description
integrator complex subunit 2
Entrez Gene ID
57508
Genome
hg19
Position
chr17:59,942,731-60,005,377
Genome
hg38
Position
chr17:61,865,370-61,928,016
MIM
611346 OMIM
HGNC
HGNC:29241 HGNC
Ensembl
ENSG00000108506 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 88
Ranking
ClinVar
0
0
0
100
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 INT2
SYNONYM KIAA1287
MIM 611346 OMIM
HGNC HGNC:29241 HGNC
Ensembl ENSG00000108506 Ensembl
AllianceGenome HGNC:29241
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000646954.1 hg38 chr17 61,910,152 61,927,977 17,826
ENST00000647009.1 hg38 chr17 61,865,390 61,927,982 62,593
ENST00000444766.7 hg38 chr17 61,865,370 61,928,016 62,647
ENST00000251334.7 hg38 chr17 61,865,367 61,927,982 62,616
ENST00000251334.7 hg19 chr17 59,942,728 60,005,343 62,616
ENST00000444766.7 hg19 chr17 59,942,731 60,005,377 62,647
ENST00000647009.1 hg19 chr17 59,942,751 60,005,343 62,593
ENST00000646954.1 hg19 chr17 59,987,513 60,005,338 17,826
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