FAM76B family with sequence similarity 76 member B

Information
Symbol
FAM76B
Type
protein-coding
Description
family with sequence similarity 76 member B
Entrez Gene ID
143684
Genome
hg19
Position
chr11:95,502,117-95,522,946
Genome
hg38
Position
chr11:95,768,953-95,789,782
HGNC
HGNC:28492 HGNC
Ensembl
ENSG00000077458 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
HGNC HGNC:28492 HGNC
Ensembl ENSG00000077458 Ensembl
AllianceGenome HGNC:28492
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000536839.1 hg38 chr11 95,770,115 95,789,561 19,447
ENST00000358780.10 hg38 chr11 95,768,953 95,789,782 20,830
ENST00000358780.10 hg19 chr11 95,502,117 95,522,946 20,830
ENST00000536839.1 hg19 chr11 95,503,279 95,522,725 19,447
Genome browser