FAM47B family with sequence similarity 47 member B

Information
Symbol
FAM47B
Type
protein-coding
Description
family with sequence similarity 47 member B
Entrez Gene ID
170062
Genome
hg19
Position
chrX:34,960,913-34,963,032
Genome
hg38
Position
chrX:34,942,796-34,944,915
HGNC
HGNC:26659 HGNC
Ensembl
ENSG00000189132 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 26
not provided 6 0
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
104
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
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:26659 HGNC
Ensembl ENSG00000189132 Ensembl
AllianceGenome HGNC:26659
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000329357.6 hg38 chrX 34,942,796 34,944,915 2,120
ENST00000329357.6 hg19 chrX 34,960,913 34,963,032 2,120
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