SUPT20HL2 SUPT20H like 2

Information
Symbol
SUPT20HL2
Type
protein-coding
Description
SUPT20H like 2
Entrez Gene ID
170067
Genome
hg19
Position
chrX:24,326,327-24,332,186
Genome
hg38
Position
chrX:24,308,210-24,314,069
HGNC
HGNC:31797 HGNC
Ensembl
ENSG00000223611 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Ranking
ClinVar
0
0
0
4
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
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 FAM48B1
SYNONYM FAM48B2
HGNC HGNC:31797 HGNC
Ensembl ENSG00000223611 Ensembl
AllianceGenome HGNC:31797
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000486479.3 hg38 chrX 24,308,210 24,314,069 5,860
ENST00000486479.3 hg19 chrX 24,326,327 24,332,186 5,860
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