VCX3A variable charge X-linked 3A

Information
Symbol
VCX3A
Type
protein-coding
Description
variable charge X-linked 3A
Entrez Gene ID
51481
Genome
hg19
Position
chrX:6,451,659-6,453,159
Genome
hg38
Position
chrX:6,533,618-6,535,118
MIM
300533 OMIM
HGNC
HGNC:18159 HGNC
Ensembl
ENSG00000169059 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 34
Conflicting classifications of pathogenicity 0 2
not provided 8 0
Uncertain significance 0 86
Ranking
ClinVar
0
0
4
120
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 VCX-8r
SYNONYM VCX-A
SYNONYM VCX3
SYNONYM VCX8R
SYNONYM VCXA
MIM 300533 OMIM
HGNC HGNC:18159 HGNC
Ensembl ENSG00000169059 Ensembl
AllianceGenome HGNC:18159
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381089.7 hg38 chrX 6,533,618 6,535,118 1,501
ENST00000398729.1 hg38 chrX 6,533,745 6,535,118 1,374
ENST00000381089.7 hg19 chrX 6,451,659 6,453,159 1,501
ENST00000398729.1 hg19 chrX 6,451,786 6,453,159 1,374
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