FAM187B family with sequence similarity 187 member B

Information
Symbol
FAM187B
Type
protein-coding
Description
family with sequence similarity 187 member B
Entrez Gene ID
148109
Genome
hg19
Position
chr19:35,715,703-35,719,642
Genome
hg38
Position
chr19:35,224,800-35,228,739
HGNC
HGNC:26366 HGNC
Ensembl
ENSG00000177558 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
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 TMEM162
HGNC HGNC:26366 HGNC
Ensembl ENSG00000177558 Ensembl
AllianceGenome HGNC:26366
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000324675.4 hg38 chr19 35,224,800 35,228,739 3,940
ENST00000324675.4 hg19 chr19 35,715,703 35,719,642 3,940
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