SUPT20H SPT20 homolog, SAGA complex component

Information
Symbol
SUPT20H
Type
protein-coding
Description
SPT20 homolog, SAGA complex component
Entrez Gene ID
55578
Genome
hg19
Position
chr13:37,583,630-37,633,786
Genome
hg38
Position
chr13:37,009,493-37,059,649
MIM
613417 OMIM
HGNC
HGNC:20596 HGNC
Ensembl
ENSG00000102710 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
risk factor 0 2
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
60
2
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 :
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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 C13
SYNONYM C13orf19
SYNONYM FAM48A
SYNONYM FP757
SYNONYM P38IP
SYNONYM SPT20
MIM 613417 OMIM
HGNC HGNC:20596 HGNC
Ensembl ENSG00000102710 Ensembl
AllianceGenome HGNC:20596
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000475892.5 hg38 chr13 37,009,493 37,059,649 50,157
ENST00000356185.7 hg38 chr13 37,009,494 37,059,650 50,157
ENST00000350612.11 hg38 chr13 37,009,312 37,059,688 50,377
ENST00000464744.5 hg38 chr13 37,009,617 37,059,432 49,816
ENST00000360252.8 hg38 chr13 37,009,316 37,059,713 50,398
ENST00000350612.11 hg19 chr13 37,583,449 37,633,825 50,377
ENST00000360252.8 hg19 chr13 37,583,453 37,633,850 50,398
ENST00000475892.5 hg19 chr13 37,583,630 37,633,786 50,157
ENST00000356185.7 hg19 chr13 37,583,631 37,633,787 50,157
ENST00000464744.5 hg19 chr13 37,583,754 37,633,569 49,816
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