H2BW1 H2B.W histone 1

Information
Symbol
H2BW1
Type
protein-coding
Description
H2B.W histone 1
Entrez Gene ID
158983
Genome
hg19
Position
chrX:103,265,719-103,268,280
Genome
hg38
Position
chrX:104,011,147-104,013,708
MIM
300507 OMIM
HGNC
HGNC:27252 HGNC
Ensembl
ENSG00000123569 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 34
Ranking
ClinVar
0
0
2
48
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
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 H2BFWT
SYNONYM TH2B-175
MIM 300507 OMIM
HGNC HGNC:27252 HGNC
Ensembl ENSG00000123569 Ensembl
AllianceGenome HGNC:27252
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000217926.7 hg38 chrX 104,011,147 104,013,708 2,562
ENST00000217926.7 hg19 chrX 103,265,719 103,268,280 2,562
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