FAM209B family with sequence similarity 209 member B

Information
Symbol
FAM209B
Type
protein-coding
Description
family with sequence similarity 209 member B
Entrez Gene ID
388799
Genome
hg19
Position
chr20:55,108,302-55,111,576
Genome
hg38
Position
chr20:56,533,246-56,536,520
HGNC
HGNC:16101 HGNC
Ensembl
ENSG00000213714 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
16
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
SYNONYM C20orf107
SYNONYM dJ1153D9.4
HGNC HGNC:16101 HGNC
Ensembl ENSG00000213714 Ensembl
AllianceGenome HGNC:16101
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000371325.1 hg38 chr20 56,533,246 56,536,520 3,275
ENST00000371325.1 hg19 chr20 55,108,302 55,111,576 3,275
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