MS4A15 membrane spanning 4-domains A15

Information
Symbol
MS4A15
Type
protein-coding
Description
membrane spanning 4-domains A15
Entrez Gene ID
219995
Genome
hg19
Position
chr11:60,524,340-60,544,206
Genome
hg38
Position
chr11:60,756,867-60,776,733
HGNC
HGNC:28573 HGNC
Ensembl
ENSG00000166961 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 9 0
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
46
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
HGNC HGNC:28573 HGNC
Ensembl ENSG00000166961 Ensembl
AllianceGenome HGNC:28573
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000528170.5 hg38 chr11 60,756,953 60,775,799 18,847
ENST00000337911.8 hg38 chr11 60,757,003 60,776,731 19,729
ENST00000405633.4 hg38 chr11 60,756,867 60,776,733 19,867
ENST00000405633.4 hg19 chr11 60,524,340 60,544,206 19,867
ENST00000528170.5 hg19 chr11 60,524,426 60,543,272 18,847
ENST00000337911.8 hg19 chr11 60,524,476 60,544,204 19,729
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