ASCC2 activating signal cointegrator 1 complex subunit 2

Information
Symbol
ASCC2
Type
protein-coding
Description
activating signal cointegrator 1 complex subunit 2
Entrez Gene ID
84164
Genome
hg19
Position
chr22:30,184,631-30,234,265
Genome
hg38
Position
chr22:29,788,642-29,838,276
MIM
614216 OMIM
HGNC
HGNC:24103 HGNC
Ensembl
ENSG00000100325 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 98
Ranking
ClinVar
0
0
0
102
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 ASC1p100
SYNONYM p100
MIM 614216 OMIM
HGNC HGNC:24103 HGNC
Ensembl ENSG00000100325 Ensembl
AllianceGenome HGNC:24103
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000307790.8 hg38 chr22 29,788,611 29,838,274 49,664
ENST00000397771.6 hg38 chr22 29,788,642 29,838,276 49,635
ENST00000542393.5 hg38 chr22 29,788,609 29,838,304 49,696
ENST00000307790.8 hg19 chr22 30,184,600 30,234,263 49,664
ENST00000397771.6 hg19 chr22 30,184,631 30,234,265 49,635
ENST00000542393.5 hg19 chr22 30,184,598 30,234,293 49,696
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