FAM86B2 family with sequence similarity 86 member B2

Information
Symbol
FAM86B2
Type
protein-coding
Description
family with sequence similarity 86 member B2
Entrez Gene ID
653333
Genome
hg19
Position
chr8:12,281,930-12,293,909
Genome
hg38
Position
chr8:12,424,421-12,436,400
MIM
616123 OMIM
HGNC
HGNC:32222 HGNC
Ensembl
ENSG00000145002 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
72
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 :
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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
MIM 616123 OMIM
HGNC HGNC:32222 HGNC
Ensembl ENSG00000145002 Ensembl
AllianceGenome HGNC:32222
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000262365.9 hg38 chr8 12,424,421 12,436,400 11,980
ENST00000262365.9 hg19 chr8 12,281,930 12,293,909 11,980
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