CLEC12B C-type lectin domain family 12 member B

Information
Symbol
CLEC12B
Type
protein-coding
Description
C-type lectin domain family 12 member B
Entrez Gene ID
387837
Genome
hg19
Position
chr12:10,163,226-10,171,395
Genome
hg38
Position
chr12:10,010,627-10,018,796
MIM
617573 OMIM
HGNC
HGNC:31966 HGNC
Ensembl
ENSG00000256660 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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
[No Data.]
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 UNQ5782
MIM 617573 OMIM
HGNC HGNC:31966 HGNC
Ensembl ENSG00000256660 Ensembl
AllianceGenome HGNC:31966
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000338896.11 hg38 chr12 10,010,627 10,018,796 8,170
ENST00000396502.5 hg38 chr12 10,010,632 10,017,948 7,317
ENST00000338896.11 hg19 chr12 10,163,226 10,171,395 8,170
ENST00000396502.5 hg19 chr12 10,163,231 10,170,547 7,317
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