SUPT20HL1 SUPT20H like 1

Information
Symbol
SUPT20HL1
Type
protein-coding
Description
SUPT20H like 1
Entrez Gene ID
100130302
Genome
hg19
Position
chrX:24,378,756-24,385,956
Genome
hg38
Position
chrX:24,360,639-24,367,839
HGNC
HGNC:30773 HGNC
Ensembl
ENSG00000223731 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
not provided 6 0
Ranking
ClinVar
0
0
0
12
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 SPT20L
HGNC HGNC:30773 HGNC
Ensembl ENSG00000223731 Ensembl
AllianceGenome HGNC:30773
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000686983.1 hg38 chrX 24,360,639 24,367,839 7,201
ENST00000436466.2 hg38 chrX 24,362,325 24,365,424 3,100
ENST00000686983.1 hg19 chrX 24,378,756 24,385,956 7,201
ENST00000436466.2 hg19 chrX 24,380,442 24,383,541 3,100
Genome browser