INTS14 integrator complex subunit 14

Information
Symbol
INTS14
Type
protein-coding
Description
integrator complex subunit 14
Entrez Gene ID
81556
Genome
hg19
Position
chr15:65,871,365-65,903,459
Genome
hg38
Position
chr15:65,579,027-65,611,121
HGNC
HGNC:25372 HGNC
Ensembl
ENSG00000138614 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
50
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 C15orf44
SYNONYM VWA9
HGNC HGNC:25372 HGNC
Ensembl ENSG00000138614 Ensembl
AllianceGenome HGNC:25372
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000420799.7 hg38 chr15 65,579,147 65,611,242 32,096
ENST00000567744.5 hg38 chr15 65,579,027 65,611,121 32,095
ENST00000313182.7 hg38 chr15 65,578,757 65,611,131 32,375
ENST00000442903.3 hg38 chr15 65,579,248 65,611,289 32,042
ENST00000652388.1 hg38 chr15 65,578,760 65,611,289 32,530
ENST00000431261.6 hg38 chr15 65,579,065 65,611,258 32,194
ENST00000569491.5 hg38 chr15 65,579,097 65,611,131 32,035
ENST00000313182.7 hg19 chr15 65,871,095 65,903,469 32,375
ENST00000567744.5 hg19 chr15 65,871,365 65,903,459 32,095
ENST00000431261.6 hg19 chr15 65,871,403 65,903,596 32,194
ENST00000420799.7 hg19 chr15 65,871,485 65,903,580 32,096
ENST00000442903.3 hg19 chr15 65,871,586 65,903,627 32,042
ENST00000569491.5 hg19 chr15 65,871,435 65,903,469 32,035
ENST00000652388.1 hg19 chr15 65,871,098 65,903,627 32,530
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