FAM162B family with sequence similarity 162 member B

Information
Symbol
FAM162B
Type
protein-coding
Description
family with sequence similarity 162 member B
Entrez Gene ID
221303
Genome
hg19
Position
chr6:117,073,360-117,086,882
Genome
hg38
Position
chr6:116,752,197-116,765,719
HGNC
HGNC:21549 HGNC
Ensembl
ENSG00000183807 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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 :
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 C6orf189
SYNONYM bA86F4.2
HGNC HGNC:21549 HGNC
Ensembl ENSG00000183807 Ensembl
AllianceGenome HGNC:21549
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368557.6 hg38 chr6 116,752,197 116,765,719 13,523
ENST00000368557.6 hg19 chr6 117,073,360 117,086,882 13,523
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