FAM181B family with sequence similarity 181 member B

Information
Symbol
FAM181B
Type
protein-coding
Description
family with sequence similarity 181 member B
Entrez Gene ID
220382
Genome
hg19
Position
chr11:82,440,982-82,444,906
Genome
hg38
Position
chr11:82,729,940-82,733,864
HGNC
HGNC:28512 HGNC
Ensembl
ENSG00000182103 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
74
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
HGNC HGNC:28512 HGNC
Ensembl ENSG00000182103 Ensembl
AllianceGenome HGNC:28512
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000329203.5 hg38 chr11 82,729,940 82,733,864 3,925
ENST00000329203.5 hg19 chr11 82,440,982 82,444,906 3,925
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