FAM168B family with sequence similarity 168 member B

Information
Symbol
FAM168B
Type
protein-coding
Description
family with sequence similarity 168 member B
Entrez Gene ID
130074
Genome
hg19
Position
chr2:131,805,449-131,851,033
Genome
hg38
Position
chr2:131,047,876-131,093,460
MIM
620078 OMIM
HGNC
HGNC:27016 HGNC
Ensembl
ENSG00000152102 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 2 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
12
2
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 MANI
MIM 620078 OMIM
HGNC HGNC:27016 HGNC
Ensembl ENSG00000152102 Ensembl
AllianceGenome HGNC:27016
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000389915.4 hg38 chr2 131,047,876 131,093,460 45,585
ENST00000409185.5 hg38 chr2 131,047,876 131,093,428 45,553
ENST00000409185.5 hg19 chr2 131,805,449 131,851,001 45,553
ENST00000389915.4 hg19 chr2 131,805,449 131,851,033 45,585
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