MS4A14 membrane spanning 4-domains A14

Information
Symbol
MS4A14
Type
protein-coding
Description
membrane spanning 4-domains A14
Entrez Gene ID
84689
Genome
hg19
Position
chr11:60,163,961-60,185,161
Genome
hg38
Position
chr11:60,396,488-60,417,688
HGNC
HGNC:30706 HGNC
Ensembl
ENSG00000166928 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 47 2
Likely benign 0 6
Uncertain significance 0 82
Ranking
ClinVar
0
0
0
88
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 MS4A16
SYNONYM NYD-SP21
HGNC HGNC:30706 HGNC
Ensembl ENSG00000166928 Ensembl
AllianceGenome HGNC:30706
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000531787.5 hg38 chr11 60,378,530 60,417,688 39,159
ENST00000395005.6 hg38 chr11 60,396,435 60,417,688 21,254
ENST00000395001.5 hg38 chr11 60,396,014 60,417,756 21,743
ENST00000300187.11 hg38 chr11 60,396,459 60,417,756 21,298
ENST00000531783.5 hg38 chr11 60,396,488 60,417,688 21,201
ENST00000531787.5 hg19 chr11 60,146,003 60,185,161 39,159
ENST00000395001.5 hg19 chr11 60,163,487 60,185,229 21,743
ENST00000395005.6 hg19 chr11 60,163,908 60,185,161 21,254
ENST00000300187.11 hg19 chr11 60,163,932 60,185,229 21,298
ENST00000531783.5 hg19 chr11 60,163,961 60,185,161 21,201
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