FAM180B family with sequence similarity 180 member B

Information
Symbol
FAM180B
Type
protein-coding
Description
family with sequence similarity 180 member B
Entrez Gene ID
399888
Genome
hg19
Position
chr11:47,608,230-47,610,746
Genome
hg38
Position
chr11:47,586,678-47,589,194
HGNC
HGNC:34451 HGNC
Ensembl
ENSG00000196666 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
20
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
HGNC HGNC:34451 HGNC
Ensembl ENSG00000196666 Ensembl
AllianceGenome HGNC:34451
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000538490.3 hg38 chr11 47,586,678 47,589,194 2,517
ENST00000538490.3 hg19 chr11 47,608,230 47,610,746 2,517
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