FAM99B family with sequence similarity 99 member B

Information
Symbol
FAM99B
Type
ncRNA
Description
family with sequence similarity 99 member B
Entrez Gene ID
100132464
Genome
hg19
Position
chr11:1,704,499-1,706,859
Genome
hg38
Position
chr11:1,683,269-1,685,629
HGNC
HGNC:32369 HGNC
Ensembl
ENSG00000205865 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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:32369 HGNC
Ensembl ENSG00000205865 Ensembl
AllianceGenome HGNC:32369
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000382166.2 hg38 chr11 1,683,269 1,685,629 2,361
ENST00000382166.2 hg19 chr11 1,704,499 1,706,859 2,361
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