VCX3B variable charge X-linked 3B

Information
Symbol
VCX3B
Type
protein-coding
Description
variable charge X-linked 3B
Entrez Gene ID
425054
Genome
hg19
Position
chrX:8,432,871-8,434,551
Genome
hg38
Position
chrX:8,464,830-8,466,510
MIM
300981 OMIM
HGNC
HGNC:31838 HGNC
Ensembl
ENSG00000205642 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 40
Conflicting classifications of pathogenicity 0 10
not provided 7 0
Uncertain significance 0 98
Ranking
ClinVar
0
0
2
136
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 VCX-C
SYNONYM VCXC
MIM 300981 OMIM
HGNC HGNC:31838 HGNC
Ensembl ENSG00000205642 Ensembl
AllianceGenome HGNC:31838
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381032.6 hg38 chrX 8,464,830 8,466,510 1,681
ENST00000381032.6 hg19 chrX 8,432,871 8,434,551 1,681
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