FAM216B family with sequence similarity 216 member B

Information
Symbol
FAM216B
Type
protein-coding
Description
family with sequence similarity 216 member B
Entrez Gene ID
144809
Genome
hg19
Position
chr13:43,355,720-43,365,685
Genome
hg38
Position
chr13:42,781,584-42,791,549
HGNC
HGNC:26883 HGNC
Ensembl
ENSG00000179813 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
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
[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
SYNONYM C13orf30
HGNC HGNC:26883 HGNC
Ensembl ENSG00000179813 Ensembl
AllianceGenome HGNC:26883
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537894.5 hg38 chr13 42,781,550 42,791,547 9,998
ENST00000313851.3 hg38 chr13 42,781,584 42,791,549 9,966
ENST00000537894.5 hg19 chr13 43,355,686 43,365,683 9,998
ENST00000313851.3 hg19 chr13 43,355,720 43,365,685 9,966
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