MAGEA12 MAGE family member A12

Information
Symbol
MAGEA12
Type
protein-coding
Description
MAGE family member A12
Entrez Gene ID
4111
Genome
hg19
Position
chrX:151,899,293-151,903,206
Genome
hg38
Position
chrX:152,733,757-152,737,669
MIM
300177 OMIM
HGNC
HGNC:6799 HGNC
Ensembl
ENSG00000213401 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
30
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 CT1.12
SYNONYM MAGE12
MIM 300177 OMIM
HGNC HGNC:6799 HGNC
Ensembl ENSG00000213401 Ensembl
AllianceGenome HGNC:6799
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000357916.8 hg38 chrX 152,733,779 152,737,669 3,891
ENST00000393869.8 hg38 chrX 152,733,757 152,737,669 3,913
ENST00000393900.4 hg38 chrX 152,733,862 152,737,106 3,245
ENST00000357916.8 hg19 chrX 151,899,293 151,903,184 3,892
ENST00000393869.8 hg19 chrX 151,899,293 151,903,206 3,914
ENST00000393900.4 hg19 chrX 151,899,856 151,903,101 3,246
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