FAM177B family with sequence similarity 177 member B

Information
Symbol
FAM177B
Type
protein-coding
Description
family with sequence similarity 177 member B
Entrez Gene ID
400823
Genome
hg19
Position
chr1:222,910,544-222,924,346
Genome
hg38
Position
chr1:222,737,202-222,751,004
HGNC
HGNC:34395 HGNC
Ensembl
ENSG00000197520 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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 :
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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
HGNC HGNC:34395 HGNC
Ensembl ENSG00000197520 Ensembl
AllianceGenome HGNC:34395
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000445590.4 hg38 chr1 222,737,202 222,751,004 13,803
ENST00000360827.6 hg38 chr1 222,737,307 222,750,196 12,890
ENST00000445590.4 hg19 chr1 222,910,544 222,924,346 13,803
ENST00000360827.6 hg19 chr1 222,910,649 222,923,538 12,890
KeyValue
strand+
start222,910,557
Gene SymbolFAM177B
Entrez GeneId400,823
Chr Band1q41
end222,924,001
chrchr1
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